Wnt1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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1002 records found for search term Wnt1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150426093	CV1184708	single nucleotide variant	NM_005430.4(WNT1):c.*9G>A	Osteogenesis imperfecta [RCV002276787]\|not provided [RCV001558901]	likely benign\|uncertain significance	12	48981649	48981649	Human	1	name
150423419	CV1184709	single nucleotide variant	NM_005430.4(WNT1):c.*116G>A	not provided [RCV001555294]	likely benign	12	48981756	48981756	Human		name
150490466	CV1208624	single nucleotide variant	NM_005430.4(WNT1):c.*143A>G	not provided [RCV001592486]	likely benign	12	48981783	48981783	Human		name
14721278	CV666722	single nucleotide variant	NM_005430.3(WNT1):c.-347C>A	not provided [RCV000831606]	benign	12	48978304	48978304	Human		name
151868220	CV1514303	single nucleotide variant	NM_005430.4(WNT1):c.104+6T>C	not provided [RCV001997994]	uncertain significance	12	48978760	48978760	Human		name
152129618	CV1650616	single nucleotide variant	NM_005430.4(WNT1):c.625-5C>T	Inborn genetic diseases [RCV003070601]\|Osteogenesis imperfecta [RCV002277036]\|not provided [RCV002118907]\|not specified [RCV004587315]	likely benign\|uncertain significance	12	48981147	48981147	Human	2	name
156030895	CV1903513	single nucleotide variant	NM_005430.4(WNT1):c.104+1G>A	not provided [RCV003100645]	pathogenic	12	48978755	48978755	Human		name
156366398	CV1909316	single nucleotide variant	NM_005430.4(WNT1):c.624+6C>G	not provided [RCV002602854]	uncertain significance	12	48980695	48980695	Human		name
155941582	CV2075992	single nucleotide variant	NM_005430.4(WNT1):c.358+5G>T	not provided [RCV002861816]	uncertain significance	12	48979726	48979726	Human		name
405270403	CV3211361	single nucleotide variant	NM_005430.4(WNT1):c.624+8T>A	WNT1-related disorder [RCV003949262]	likely benign	12	48980697	48980697	Human		name , trait , alternate_id
597976109	CV3829112	single nucleotide variant	NM_005430.4(WNT1):c.105-1G>A	not provided [RCV005169561]	likely pathogenic	12	48979467	48979467	Human		name
8611921	CV59405	single nucleotide variant	NM_005430.4(WNT1):c.624+4A>G	Osteogenesis imperfecta type 15 [RCV000043493]	pathogenic	12	48980693	48980693	Human	1	name , alternate_id
15152805	CV760209	single nucleotide variant	NM_005430.4(WNT1):c.105-6C>T	Inborn genetic diseases [RCV002542177]\|not provided [RCV000923942]	likely benign\|uncertain significance	12	48979462	48979462	Human	1	name
152149074	CV1566448	deletion	NM_005430.4(WNT1):c.358+13del	not provided [RCV002139243]	likely benign	12	48979733	48979733	Human		name
152069463	CV1589208	single nucleotide variant	NM_005430.4(WNT1):c.625-17T>C	not provided [RCV002209791]	likely benign	12	48981135	48981135	Human		name
156329818	CV1992688	single nucleotide variant	NM_005430.4(WNT1):c.359-13C>T	not provided [RCV002649758]	likely benign	12	48980411	48980411	Human		name
402497607	CV3005935	single nucleotide variant	NM_005430.4(WNT1):c.358+17G>C	not provided [RCV003688088]	likely benign	12	48979738	48979738	Human		name
405144967	CV3126092	single nucleotide variant	NM_005430.4(WNT1):c.625-18C>T	not provided [RCV003817008]	likely benign	12	48981134	48981134	Human		name
405028094	CV3129705	single nucleotide variant	NM_005430.4(WNT1):c.358+14A>C	not provided [RCV003830303]	likely benign	12	48979735	48979735	Human		name
405250930	CV3180775	deletion	NM_005430.4(WNT1):c.625-11del	not provided [RCV003870052]	likely benign	12	48981141	48981141	Human		name
597941445	CV3757400	single nucleotide variant	NM_005430.4(WNT1):c.358+17G>T	not provided [RCV005077586]	likely benign	12	48979738	48979738	Human		name
150481908	CV1209873	single nucleotide variant	NM_005430.4(WNT1):c.105-219C>G	not provided [RCV001590571]	likely benign	12	48979249	48979249	Human		name
153347157	CV1694460	single nucleotide variant	NM_005430.4(WNT1):c.27C>T (p.Gly9=)	Osteogenesis imperfecta [RCV002277857]\|not provided [RCV005058219]	likely benign\|uncertain significance	12	48978677	48978677	Human	1	name
401907196	CV2804846	deletion	NM_005430.4(WNT1):c.6del (p.Leu3fs)	WNT1-related disorder [RCV003422478]	likely pathogenic	12	48978653	48978653	Human		name , trait , alternate_id
405199614	CV3164504	single nucleotide variant	NM_005430.4(WNT1):c.15G>T (p.Ala5=)	not provided [RCV003860561]	likely benign	12	48978665	48978665	Human		name
13786148	CV481176	deletion	NM_005430.4(WNT1):c.104+4_104+44del	Osteogenesis imperfecta type 15 [RCV000677241]	likely pathogenic	12	48978757	48978797	Human	1	name , alternate_id
155918332	CV1981070	deletion	NM_005430.4(WNT1):c.358+18_358+29del	not provided [RCV002614427]	likely benign	12	48979737	48979748	Human		name
155989872	CV1990439	single nucleotide variant	NM_005430.4(WNT1):c.93T>C (p.Ser31=)	not provided [RCV002617974]	likely benign	12	48978743	48978743	Human		name
156287808	CV2172387	single nucleotide variant	NM_005430.4(WNT1):c.3G>A (p.Met1Ile)	not provided [RCV003027557]	pathogenic	12	48978653	48978653	Human		name
401768253	CV2735238	single nucleotide variant	NM_005430.4(WNT1):c.8T>A (p.Leu3His)	Inborn genetic diseases [RCV003302509]	likely benign	12	48978658	48978658	Human	1	name
597863325	CV3814012	single nucleotide variant	NM_005430.4(WNT1):c.87C>T (p.Asn29=)	not provided [RCV005147081]	likely benign	12	48978737	48978737	Human		name
153347156	CV1694459	single nucleotide variant	NM_005430.4(WNT1):c.23C>T (p.Pro8Leu)	Osteogenesis imperfecta [RCV002277856]	uncertain significance	12	48978673	48978673	Human	1	name
405143975	CV2946073	single nucleotide variant	NM_005430.4(WNT1):c.132G>A (p.Thr44=)	not provided [RCV003669507]	uncertain significance	12	48979495	48979495	Human		name
405090998	CV3167899	single nucleotide variant	NM_005430.4(WNT1):c.111T>C (p.Ile37=)	not provided [RCV003852289]	likely benign	12	48979474	48979474	Human		name
598127509	CV3882708	duplication	NM_005430.4(WNT1):c.69dup (p.Ala24fs)	not provided [RCV005234239]	likely pathogenic	12	48978716	48978717	Human		name
15184316	CV725114	single nucleotide variant	NM_005430.4(WNT1):c.255G>A (p.Gly85=)	not provided [RCV000886419]	likely benign	12	48979618	48979618	Human		name
15151357	CV753403	single nucleotide variant	NM_005430.4(WNT1):c.159G>A (p.Leu53=)	WNT1-related disorder [RCV003960425]\|not provided [RCV000923658]	likely benign	12	48979522	48979522	Human	1	name , alternate_id
15134766	CV753404	single nucleotide variant	NM_005430.4(WNT1):c.237G>A (p.Leu79=)	not provided [RCV000920742]	likely benign	12	48979600	48979600	Human		name
150555989	CV1295359	deletion	NM_005430.4(WNT1):c.258del (p.Gln87fs)	not provided [RCV001773794]	uncertain significance	12	48979621	48979621	Human		name
151833638	CV1388491	single nucleotide variant	NM_005430.4(WNT1):c.52G>T (p.Ala18Ser)	not provided [RCV001955927]	uncertain significance	12	48978702	48978702	Human		name
152168538	CV1548059	single nucleotide variant	NM_005430.4(WNT1):c.441C>T (p.Ser147=)	not provided [RCV002161155]	likely benign	12	48980506	48980506	Human		name
152155746	CV1561009	single nucleotide variant	NM_005430.4(WNT1):c.975C>T (p.Cys325=)	not provided [RCV002102903]	likely benign	12	48981502	48981502	Human		name
152027288	CV1562693	single nucleotide variant	NM_005430.4(WNT1):c.318T>C (p.Thr106=)	WNT1-related disorder [RCV003903332]\|not provided [RCV002104843]	likely benign	12	48979681	48979681	Human	1	name , alternate_id
152161619	CV1584530	single nucleotide variant	NM_005430.4(WNT1):c.480C>T (p.Pro160=)	not provided [RCV002123302]	likely benign	12	48980545	48980545	Human		name
152119348	CV1587623	single nucleotide variant	NM_005430.4(WNT1):c.414G>T (p.Ser138=)	not provided [RCV002081337]	benign	12	48980479	48980479	Human		name
152073653	CV1615482	single nucleotide variant	NM_005430.4(WNT1):c.456G>T (p.Thr152=)	Inborn genetic diseases [RCV004965785]\|not provided [RCV002091930]	likely benign	12	48980521	48980521	Human	1	name
153347864	CV1694912	single nucleotide variant	NM_005430.4(WNT1):c.726G>A (p.Val242=)	Connective tissue disorder [RCV002278843]	uncertain significance	12	48981253	48981253	Human	1	name
156340536	CV1902672	single nucleotide variant	NM_005430.4(WNT1):c.504G>C (p.Gly168=)	not provided [RCV003090336]	likely benign	12	48980569	48980569	Human		name
155946065	CV1911310	single nucleotide variant	NM_005430.4(WNT1):c.435A>G (p.Glu145=)	not provided [RCV002615940]	likely benign	12	48980500	48980500	Human		name
156407946	CV1911389	single nucleotide variant	NM_005430.4(WNT1):c.466C>A (p.Arg156=)	not provided [RCV002607061]	likely benign	12	48980531	48980531	Human		name
156408310	CV1911556	single nucleotide variant	NM_005430.4(WNT1):c.990C>T (p.Cys330=)	not provided [RCV002607189]	likely benign	12	48981517	48981517	Human		name
156408314	CV1911557	single nucleotide variant	NM_005430.4(WNT1):c.994A>C (p.Arg332=)	not provided [RCV002607190]	likely benign	12	48981521	48981521	Human		name
156438572	CV1947181	single nucleotide variant	NM_005430.4(WNT1):c.723C>G (p.Ala241=)	not provided [RCV003108516]	likely benign	12	48981250	48981250	Human		name
156252016	CV1963822	single nucleotide variant	NM_005430.4(WNT1):c.52G>A (p.Ala18Thr)	Inborn genetic diseases [RCV004064408]\|not provided [RCV002576571]\|not specified [RCV004700775]	uncertain significance	12	48978702	48978702	Human	1	name
156194518	CV2018076	single nucleotide variant	NM_005430.4(WNT1):c.375G>A (p.Ala125=)	not provided [RCV002700067]	likely benign	12	48980440	48980440	Human		name
155998620	CV2045411	single nucleotide variant	NM_005430.4(WNT1):c.741C>A (p.Arg247=)	not provided [RCV002756089]	likely benign	12	48981268	48981268	Human		name
156342813	CV2123920	single nucleotide variant	NM_005430.4(WNT1):c.528C>T (p.Phe176=)	not provided [RCV002938990]	likely benign	12	48980593	48980593	Human		name
156128144	CV2155499	single nucleotide variant	NM_005430.4(WNT1):c.927C>A (p.Gly309=)	not provided [RCV003003251]	likely benign	12	48981454	48981454	Human		name
156100381	CV2164310	single nucleotide variant	NM_005430.4(WNT1):c.315C>T (p.Pro105=)	not provided [RCV003038560]	likely benign	12	48979678	48979678	Human		name
156134226	CV2181413	single nucleotide variant	NM_005430.4(WNT1):c.663C>T (p.His221=)	not provided [RCV003039807]	likely benign	12	48981190	48981190	Human		name
243062165	CV2414373	deletion	NM_005430.4(WNT1):c.255del (p.Leu86fs)	Osteogenesis imperfecta type 15 [RCV003139442]	pathogenic	12	48979613	48979613	Human	1	name , alternate_id
405168776	CV2854087	single nucleotide variant	NM_005430.4(WNT1):c.355C>A (p.Arg119=)	not provided [RCV003541998]	likely benign	12	48979718	48979718	Human		name
405079066	CV2945369	single nucleotide variant	NM_005430.4(WNT1):c.429C>T (p.Cys143=)	not provided [RCV003664416]	likely benign	12	48980494	48980494	Human		name
405149082	CV2959546	single nucleotide variant	NM_005430.4(WNT1):c.846A>G (p.Lys282=)	not provided [RCV003673870]	likely benign	12	48981373	48981373	Human		name
405198173	CV3032759	single nucleotide variant	NM_005430.4(WNT1):c.765C>A (p.Arg255=)	not provided [RCV003707167]	likely benign	12	48981292	48981292	Human		name
405133107	CV3047489	single nucleotide variant	NM_005430.4(WNT1):c.807G>T (p.Ala269=)	not provided [RCV003725005]	likely benign	12	48981334	48981334	Human		name
405096111	CV3119055	single nucleotide variant	NM_005430.4(WNT1):c.98G>T (p.Arg33Leu)	not provided [RCV003811506]	uncertain significance	12	48978748	48978748	Human		name
404979387	CV3127811	single nucleotide variant	NM_005430.4(WNT1):c.858C>A (p.Pro286=)	not provided [RCV003825843]	likely benign	12	48981385	48981385	Human		name
405146744	CV3141820	single nucleotide variant	NM_005430.4(WNT1):c.339C>T (p.Phe113=)	not provided [RCV003839742]	likely benign	12	48979702	48979702	Human		name
405174413	CV3148152	single nucleotide variant	NM_005430.4(WNT1):c.858C>G (p.Pro286=)	not provided [RCV003858124]	likely benign	12	48981385	48981385	Human		name
405189201	CV3149539	single nucleotide variant	NM_005430.4(WNT1):c.80C>T (p.Ala27Val)	not provided [RCV003843265]	uncertain significance	12	48978730	48978730	Human		name
405234125	CV3158009	single nucleotide variant	NM_005430.4(WNT1):c.912C>T (p.Arg304=)	not provided [RCV003865765]	likely benign	12	48981439	48981439	Human		name
405704091	CV3224999	duplication	NM_005430.4(WNT1):c.216dup (p.Arg73fs)	Osteogenesis imperfecta type 15 [RCV003989955]	uncertain significance	12	48979578	48979579	Human	1	name , alternate_id
597846049	CV3736557	single nucleotide variant	NM_005430.4(WNT1):c.960C>T (p.Pro320=)	not provided [RCV005065716]	likely benign	12	48981487	48981487	Human		name
597940265	CV3788967	single nucleotide variant	NM_005430.4(WNT1):c.936G>C (p.Gly312=)	not provided [RCV005133430]	likely benign	12	48981463	48981463	Human		name
13478986	CV445017	single nucleotide variant	NM_005430.4(WNT1):c.624G>A (p.Thr208=)	Osteogenesis imperfecta [RCV005250069]\|not provided [RCV000520830]	uncertain significance	12	48980689	48980689	Human	1	name
14741851	CV656169	single nucleotide variant	NM_005430.4(WNT1):c.576G>A (p.Arg192=)	not provided [RCV000840976]	likely benign	12	48980641	48980641	Human		name
15109967	CV753405	single nucleotide variant	NM_005430.4(WNT1):c.711C>T (p.Pro237=)	not provided [RCV000916441]	likely benign	12	48981238	48981238	Human		name
15193428	CV769145	single nucleotide variant	NM_005430.4(WNT1):c.753C>T (p.Asp251=)	not provided [RCV000933359]	likely benign	12	48981280	48981280	Human		name
15187366	CV769146	single nucleotide variant	NM_005430.4(WNT1):c.798T>C (p.Ala266=)	not provided [RCV000931636]	likely benign	12	48981325	48981325	Human		name
15197949	CV769147	single nucleotide variant	NM_005430.4(WNT1):c.820C>T (p.Leu274=)	not provided [RCV000934664]	likely benign	12	48981347	48981347	Human		name
15127419	CV784400	single nucleotide variant	NM_005430.4(WNT1):c.462C>T (p.Asp154=)	not provided [RCV000980543]	likely benign	12	48980527	48980527	Human		name
150456338	CV1214404	deletion	NM_005430.4(WNT1):c.480del (p.Gly162fs)	not provided [RCV001597503]	likely pathogenic	12	48980542	48980542	Human		name
151351348	CV1323492	duplication	NM_005430.4(WNT1):c.506dup (p.Cys170fs)	Osteogenesis imperfecta [RCV002271673]\|Osteogenesis imperfecta type 15 [RCV001806348]\|not provided [RCV001869564]	pathogenic	12	48980564	48980565	Human	2	name , alternate_id
151805474	CV1371983	single nucleotide variant	NM_005430.4(WNT1):c.179G>A (p.Ser60Asn)	not provided [RCV001953318]	uncertain significance	12	48979542	48979542	Human		name
151819680	CV1385890	single nucleotide variant	NM_005430.4(WNT1):c.250G>T (p.Gly84Trp)	not provided [RCV002013251]	uncertain significance	12	48979613	48979613	Human		name
151862416	CV1420214	single nucleotide variant	NM_005430.4(WNT1):c.253G>A (p.Gly85Arg)	not provided [RCV001980292]	uncertain significance	12	48979616	48979616	Human		name
151820072	CV1450151	duplication	NM_005430.4(WNT1):c.499dup (p.Trp167fs)	not provided [RCV001879129]	pathogenic	12	48980563	48980564	Human		name
151717172	CV1465166	single nucleotide variant	NM_005430.4(WNT1):c.265G>A (p.Ala89Thr)	not provided [RCV002003096]	uncertain significance	12	48979628	48979628	Human		name
152979438	CV1675560	duplication	NM_005430.4(WNT1):c.860dup (p.His287fs)	Osteogenesis imperfecta type 15 [RCV002244150]	likely pathogenic	12	48981386	48981387	Human	1	name , alternate_id
156410745	CV1958506	single nucleotide variant	NM_005430.4(WNT1):c.251G>A (p.Gly84Glu)	not provided [RCV002587253]	uncertain significance	12	48979614	48979614	Human		name
156220637	CV1981274	single nucleotide variant	NM_005430.4(WNT1):c.178A>T (p.Ser60Cys)	not provided [RCV002626433]	uncertain significance	12	48979541	48979541	Human		name
156377918	CV2024914	single nucleotide variant	NM_005430.4(WNT1):c.1095A>C (p.Val365=)	not provided [RCV002722078]	likely benign	12	48981622	48981622	Human		name
10449639	CV215450	single nucleotide variant	NM_005430.4(WNT1):c.264T>A (p.Ser88Arg)	Osteogenesis imperfecta [RCV002277561]\|Osteogenesis imperfecta type 15 [RCV002494517]\|not provided [RCV000893654]\|not specified [RCV000202661]	benign\|likely benign\|conflicting interpretations of pathogenicity	12	48979627	48979627	Human	2	name , alternate_id
156346069	CV2191194	single nucleotide variant	NM_005430.4(WNT1):c.112G>A (p.Val38Met)	not provided [RCV003048017]	uncertain significance	12	48979475	48979475	Human		name
156134087	CV2196002	single nucleotide variant	NM_005430.4(WNT1):c.118G>A (p.Val40Ile)	Inborn genetic diseases [RCV002640870]\|not provided [RCV005099436]	uncertain significance	12	48979481	48979481	Human	1	name
243059375	CV2405974	duplication	NM_005430.4(WNT1):c.331dup (p.His111fs)	Osteogenesis imperfecta type 15 [RCV003134801]	likely pathogenic	12	48979690	48979691	Human	1	name , alternate_id
402519470	CV2871036	deletion	NM_005430.4(WNT1):c.578del (p.Asp193fs)	Inborn genetic diseases [RCV004676215]\|not provided [RCV003547647]	pathogenic	12	48980643	48980643	Human	1	name
405022479	CV2877525	deletion	NM_005430.4(WNT1):c.707del (p.Leu236fs)	not provided [RCV003577721]	pathogenic	12	48981234	48981234	Human		name
405171539	CV2897532	single nucleotide variant	NM_005430.4(WNT1):c.102G>A (p.Trp34Ter)	not provided [RCV003563163]	pathogenic	12	48978752	48978752	Human		name
402487825	CV2928479	single nucleotide variant	NM_005430.4(WNT1):c.269T>C (p.Val90Ala)	not provided [RCV003572636]	uncertain significance	12	48979632	48979632	Human		name
405058800	CV2928988	deletion	NM_005430.4(WNT1):c.547del (p.Glu183fs)	not provided [RCV003580319]	pathogenic	12	48980610	48980610	Human		name
405172395	CV2961348	single nucleotide variant	NM_005430.4(WNT1):c.287A>G (p.Gln96Arg)	not provided [RCV003675459]	uncertain significance	12	48979650	48979650	Human		name
405129158	CV2962201	single nucleotide variant	NM_005430.4(WNT1):c.244G>C (p.Val82Leu)	not provided [RCV003668223]	uncertain significance	12	48979607	48979607	Human		name
405160821	CV3061667	single nucleotide variant	NM_005430.4(WNT1):c.227C>G (p.Pro76Arg)	not provided [RCV003726971]	uncertain significance	12	48979590	48979590	Human		name
405129010	CV3133239	single nucleotide variant	NM_005430.4(WNT1):c.196C>T (p.Arg66Cys)	not provided [RCV003838209]	uncertain significance	12	48979559	48979559	Human		name
405183016	CV3147928	single nucleotide variant	NM_005430.4(WNT1):c.119T>C (p.Val40Ala)	not provided [RCV003842638]	uncertain significance	12	48979482	48979482	Human		name
405249910	CV3180582	single nucleotide variant	NM_005430.4(WNT1):c.154A>G (p.Ser52Gly)	Inborn genetic diseases [RCV004968538]\|not provided [RCV003869859]	uncertain significance	12	48979517	48979517	Human	1	name
405250139	CV3180648	single nucleotide variant	NM_005430.4(WNT1):c.174G>T (p.Glu58Asp)	not provided [RCV003869925]	uncertain significance	12	48979537	48979537	Human		name
407501955	CV3495640	deletion	NM_005430.4(WNT1):c.506del (p.Gly169fs)	not provided [RCV004697480]	likely pathogenic	12	48980565	48980565	Human		name
408390842	CV3527784	single nucleotide variant	NM_005430.4(WNT1):c.152A>G (p.Lys51Arg)	Inborn genetic diseases [RCV004968643]\|not provided [RCV004775053]	uncertain significance	12	48979515	48979515	Human	1	name
597704513	CV3714082	deletion	NM_005430.4(WNT1):c.393del (p.Ser132fs)	Osteogenesis imperfecta type 15 [RCV005009104]	likely pathogenic	12	48980457	48980457	Human	1	name , alternate_id
597953147	CV3756656	single nucleotide variant	NM_005430.4(WNT1):c.172G>C (p.Glu58Gln)	not provided [RCV005079714]	uncertain significance	12	48979535	48979535	Human		name
597856884	CV3758856	single nucleotide variant	NM_005430.4(WNT1):c.117C>A (p.Asn39Lys)	not provided [RCV005088816]	uncertain significance	12	48979480	48979480	Human		name
597961514	CV3840754	single nucleotide variant	NM_005430.4(WNT1):c.169C>G (p.Leu57Val)	not provided [RCV005193047]	uncertain significance	12	48979532	48979532	Human		name
598275506	CV3937151	single nucleotide variant	NM_005430.4(WNT1):c.185A>C (p.Gln62Pro)	Inborn genetic diseases [RCV005304640]	uncertain significance	12	48979548	48979548	Human	1	name
8611920	CV59404	duplication	NM_005430.4(WNT1):c.859dup (p.His287fs)	OSTEOPOROSIS, EARLY-ONSET, SUSCEPTIBILITY TO [RCV000043492]\|Osteogenesis imperfecta type 15 [RCV000043491]	pathogenic\|risk factor	12	48981380	48981381	Human	2	name , alternate_id
150417887	CV1198383	single nucleotide variant	NM_005430.4(WNT1):c.793C>A (p.Arg265Ser)	Inborn genetic diseases [RCV002573238]\|not provided [RCV001576501]	uncertain significance	12	48981320	48981320	Human	1	name
150459291	CV1202904	single nucleotide variant	NM_005430.4(WNT1):c.506G>A (p.Gly169Asp)	Inborn genetic diseases [RCV002569120]\|Osteogenesis imperfecta [RCV002276822]\|Osteogenesis imperfecta type 15 [RCV005005975]\|WNT1-related disorder [RCV003416401]\|not provided [RCV001586557]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	12	48980571	48980571	Human	4	name , alternate_id
150520394	CV1289578	single nucleotide variant	NM_005430.4(WNT1):c.617G>A (p.Gly206Asp)	Osteogenesis imperfecta type 15 [RCV001729995]	likely pathogenic	12	48980682	48980682	Human	1	name , alternate_id
150553051	CV1298065	single nucleotide variant	NM_005430.4(WNT1):c.673G>A (p.Gly225Ser)	not provided [RCV001768678]	uncertain significance	12	48981200	48981200	Human		name
150549812	CV1299891	single nucleotide variant	NM_005430.4(WNT1):c.730G>T (p.Asp244Tyr)	not provided [RCV001765360]	uncertain significance	12	48981257	48981257	Human		name
150541530	CV1301510	single nucleotide variant	NM_005430.4(WNT1):c.661C>T (p.His221Tyr)	not provided [RCV001760976]\|not specified [RCV005237967]	uncertain significance	12	48981188	48981188	Human		name
150528347	CV1301856	single nucleotide variant	NM_005430.4(WNT1):c.467G>A (p.Arg156Gln)	not provided [RCV001755228]	uncertain significance	12	48980532	48980532	Human		name
151757756	CV1340434	single nucleotide variant	NM_005430.4(WNT1):c.775G>C (p.Gly259Arg)	not provided [RCV001913629]	uncertain significance	12	48981302	48981302	Human		name
151875248	CV1376061	single nucleotide variant	NM_005430.4(WNT1):c.514G>A (p.Asp172Asn)	not provided [RCV002019459]	uncertain significance	12	48980579	48980579	Human		name
151856962	CV1377518	single nucleotide variant	NM_005430.4(WNT1):c.502G>C (p.Gly168Arg)	not provided [RCV001923516]	uncertain significance	12	48980567	48980567	Human		name
151726586	CV1387197	single nucleotide variant	NM_005430.4(WNT1):c.403G>A (p.Val135Ile)	not provided [RCV001910414]	uncertain significance	12	48980468	48980468	Human		name
151743723	CV1404532	single nucleotide variant	NM_005430.4(WNT1):c.541G>A (p.Gly181Ser)	Inborn genetic diseases [RCV003170548]\|not provided [RCV002022584]\|not specified [RCV004699636]	uncertain significance	12	48980606	48980606	Human	1	name
151740956	CV1404801	single nucleotide variant	NM_005430.4(WNT1):c.980T>G (p.Leu327Arg)	Inborn genetic diseases [RCV002550391]\|not provided [RCV001947099]	uncertain significance	12	48981507	48981507	Human	1	name
151753310	CV1407268	single nucleotide variant	NM_005430.4(WNT1):c.794G>C (p.Arg265Pro)	not provided [RCV002023612]	uncertain significance	12	48981321	48981321	Human		name
151728002	CV1409951	single nucleotide variant	NM_005430.4(WNT1):c.689G>A (p.Arg230His)	Inborn genetic diseases [RCV004044030]\|Osteogenesis imperfecta [RCV002276932]\|not provided [RCV001910580]	uncertain significance	12	48981216	48981216	Human	2	name
151773292	CV1414409	single nucleotide variant	NM_005430.4(WNT1):c.626C>T (p.Thr209Ile)	not provided [RCV001874655]	uncertain significance	12	48981153	48981153	Human		name
151776569	CV1440344	single nucleotide variant	NM_005430.4(WNT1):c.681C>A (p.Cys227Ter)	Osteogenesis imperfecta type 15 [RCV005006132]\|not provided [RCV001874965]	pathogenic\|likely pathogenic	12	48981208	48981208	Human	1	name , alternate_id
151816756	CV1441053	single nucleotide variant	NM_005430.4(WNT1):c.907G>T (p.Gly303Ter)	not provided [RCV001933749]	pathogenic	12	48981434	48981434	Human		name
151818260	CV1453480	single nucleotide variant	NM_005430.4(WNT1):c.953C>G (p.Ser318Trp)	not provided [RCV001900626]	uncertain significance	12	48981480	48981480	Human		name
151740447	CV1455330	single nucleotide variant	NM_005430.4(WNT1):c.874T>G (p.Phe292Val)	Inborn genetic diseases [RCV005301059]\|not provided [RCV002005767]	uncertain significance	12	48981401	48981401	Human	1	name
151851746	CV1458868	single nucleotide variant	NM_005430.4(WNT1):c.589C>T (p.Leu197Phe)	not provided [RCV002016679]	uncertain significance	12	48980654	48980654	Human		name
151889394	CV1479654	single nucleotide variant	NM_005430.4(WNT1):c.409C>T (p.His137Tyr)	Inborn genetic diseases [RCV004970374]\|not provided [RCV001888167]	uncertain significance	12	48980474	48980474	Human	1	name
151729299	CV1483146	single nucleotide variant	NM_005430.4(WNT1):c.944G>T (p.Cys315Phe)	not provided [RCV001892076]	uncertain significance	12	48981471	48981471	Human		name
151882080	CV1484456	single nucleotide variant	NM_005430.4(WNT1):c.859C>T (p.His287Tyr)	not provided [RCV001941212]	uncertain significance	12	48981386	48981386	Human		name
151846397	CV1488210	single nucleotide variant	NM_005430.4(WNT1):c.384C>A (p.Phe128Leu)	WNT1-related disorder [RCV003893034]\|not provided [RCV001995390]	uncertain significance	12	48980449	48980449	Human	1	name , alternate_id
151879175	CV1490785	single nucleotide variant	NM_005430.4(WNT1):c.305G>C (p.Trp102Ser)	not provided [RCV001940777]	uncertain significance	12	48979668	48979668	Human		name
152033677	CV1669023	single nucleotide variant	NM_005430.4(WNT1):c.495G>T (p.Trp165Cys)	not provided [RCV002223366]	uncertain significance	12	48980560	48980560	Human		name
152999568	CV1679910	single nucleotide variant	NM_005430.4(WNT1):c.893T>G (p.Phe298Cys)	Osteogenesis imperfecta type 15 [RCV002251300]	likely pathogenic	12	48981420	48981420	Human	1	name , alternate_id
153347159	CV1694461	single nucleotide variant	NM_005430.4(WNT1):c.535C>T (p.Leu179Phe)	Inborn genetic diseases [RCV003096245]\|Osteogenesis imperfecta [RCV002277858]\|not provided [RCV003546749]	uncertain significance	12	48980600	48980600	Human	2	name
155643170	CV1706582	single nucleotide variant	NM_005430.4(WNT1):c.465C>A (p.Tyr155Ter)	See cases [RCV004584491]	pathogenic	12	48980530	48980530	Human		name
155665179	CV1773304	single nucleotide variant	NM_005430.4(WNT1):c.607A>T (p.Asn203Tyr)	not provided [RCV002297016]	uncertain significance	12	48980672	48980672	Human		name
155722784	CV1773548	single nucleotide variant	NM_005430.4(WNT1):c.644G>C (p.Arg215Pro)	not provided [RCV002301357]	uncertain significance	12	48981171	48981171	Human		name
9693673	CV178389	deletion	NM_005430.4(WNT1):c.1026del (p.Glu343fs)	Osteogenesis imperfecta type 15 [RCV000157063]\|not provided [RCV003556208]	pathogenic	12	48981552	48981552	Human	1	name , alternate_id
156367562	CV1902849	single nucleotide variant	NM_005430.4(WNT1):c.899C>A (p.Thr300Lys)	not provided [RCV003092168]	uncertain significance	12	48981426	48981426	Human		name
156218455	CV1903514	single nucleotide variant	NM_005430.4(WNT1):c.371C>T (p.Thr124Met)	not provided [RCV003084895]\|not specified [RCV004690368]	uncertain significance	12	48980436	48980436	Human		name
156400650	CV1907873	single nucleotide variant	NM_005430.4(WNT1):c.755G>C (p.Gly252Ala)	Inborn genetic diseases [RCV004963449]\|not provided [RCV002584839]	uncertain significance	12	48981282	48981282	Human	1	name
156207472	CV1913283	single nucleotide variant	NM_005430.4(WNT1):c.593T>C (p.Met198Thr)	not provided [RCV002595938]	uncertain significance	12	48980658	48980658	Human		name
156374894	CV1933069	single nucleotide variant	NM_005430.4(WNT1):c.644G>T (p.Arg215Leu)	not provided [RCV002633742]	uncertain significance	12	48981171	48981171	Human		name
156356626	CV1962457	single nucleotide variant	NM_005430.4(WNT1):c.349G>A (p.Val117Ile)	not provided [RCV002581435]	uncertain significance	12	48979712	48979712	Human		name
156167734	CV1993439	single nucleotide variant	NM_005430.4(WNT1):c.607A>G (p.Asn203Asp)	not provided [RCV002642629]	uncertain significance	12	48980672	48980672	Human		name
155947493	CV1996421	single nucleotide variant	NM_005430.4(WNT1):c.730G>A (p.Asp244Asn)	Inborn genetic diseases [RCV002667974]\|not provided [RCV002685828]	uncertain significance	12	48981257	48981257	Human	1	name
156100852	CV2001071	single nucleotide variant	NM_005430.4(WNT1):c.572G>C (p.Gly191Ala)	not provided [RCV002639577]	uncertain significance	12	48980637	48980637	Human		name
156128335	CV2012566	single nucleotide variant	NM_005430.4(WNT1):c.725T>C (p.Val242Ala)	not provided [RCV002696305]	uncertain significance	12	48981252	48981252	Human		name
156027255	CV2055902	single nucleotide variant	NM_005430.4(WNT1):c.988T>C (p.Cys330Arg)	not provided [RCV002820904]	uncertain significance	12	48981515	48981515	Human		name
156021321	CV2081511	single nucleotide variant	NM_005430.4(WNT1):c.704G>T (p.Arg235Leu)	not provided [RCV002866622]	uncertain significance	12	48981231	48981231	Human		name
156365088	CV2167242	single nucleotide variant	NM_005430.4(WNT1):c.570G>T (p.Lys190Asn)	not provided [RCV003031832]	uncertain significance	12	48980635	48980635	Human		name
156330609	CV2171743	single nucleotide variant	NM_005430.4(WNT1):c.976G>A (p.Glu326Lys)	not provided [RCV003029748]	uncertain significance	12	48981503	48981503	Human		name
156365194	CV2192086	single nucleotide variant	NM_005430.4(WNT1):c.623C>A (p.Thr208Lys)	not provided [RCV003065904]	uncertain significance	12	48980688	48980688	Human		name
156039625	CV2219400	single nucleotide variant	NM_005430.4(WNT1):c.876C>G (p.Phe292Leu)	Inborn genetic diseases [RCV002692168]	uncertain significance	12	48981403	48981403	Human	1	name
155930057	CV2224656	single nucleotide variant	NM_005430.4(WNT1):c.485G>A (p.Gly162Asp)	Inborn genetic diseases [RCV002728623]	uncertain significance	12	48980550	48980550	Human	1	name
156064395	CV2240226	single nucleotide variant	NM_005430.4(WNT1):c.575G>A (p.Arg192Gln)	Inborn genetic diseases [RCV002782801]	uncertain significance	12	48980640	48980640	Human	1	name
156172982	CV2293438	single nucleotide variant	NM_005430.4(WNT1):c.859C>G (p.His287Asp)	Inborn genetic diseases [RCV002891509]	uncertain significance	12	48981386	48981386	Human	1	name
401731052	CV2686858	single nucleotide variant	NM_005430.4(WNT1):c.913C>G (p.Leu305Val)	Inborn genetic diseases [RCV003289755]	uncertain significance	12	48981440	48981440	Human	1	name
401913659	CV2799011	single nucleotide variant	NM_005430.4(WNT1):c.823G>A (p.Glu275Lys)	WNT1-related disorder [RCV003400199]	uncertain significance	12	48981350	48981350	Human		name , trait , alternate_id
402505517	CV2880009	single nucleotide variant	NM_005430.4(WNT1):c.884C>T (p.Ser295Leu)	not provided [RCV003546217]	uncertain significance	12	48981411	48981411	Human		name
405109871	CV2898856	single nucleotide variant	NM_005430.4(WNT1):c.505G>T (p.Gly169Cys)	Osteogenesis imperfecta [RCV004765889]\|not provided [RCV003557721]	likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	12	48980570	48980570	Human	1	name
405109880	CV2898857	single nucleotide variant	NM_005430.4(WNT1):c.529G>T (p.Gly177Cys)	not provided [RCV003557722]	likely pathogenic	12	48980594	48980594	Human		name
405180414	CV2908568	single nucleotide variant	NM_005430.4(WNT1):c.571G>A (p.Gly191Arg)	not provided [RCV003563859]	uncertain significance	12	48980636	48980636	Human		name
402472136	CV2912162	single nucleotide variant	NM_005430.4(WNT1):c.513C>G (p.Ser171Arg)	not provided [RCV003570723]	uncertain significance	12	48980578	48980578	Human		name
402465402	CV2916532	single nucleotide variant	NM_005430.4(WNT1):c.422G>C (p.Arg141Pro)	not provided [RCV003569141]	uncertain significance	12	48980487	48980487	Human		name
405131078	CV2962474	single nucleotide variant	NM_005430.4(WNT1):c.923C>T (p.Ala308Val)	not provided [RCV003668382]	uncertain significance	12	48981450	48981450	Human		name
405186789	CV2964094	single nucleotide variant	NM_005430.4(WNT1):c.619C>T (p.Arg207Cys)	not provided [RCV003676825]	uncertain significance	12	48980684	48980684	Human		name
405229761	CV2968062	single nucleotide variant	NM_005430.4(WNT1):c.437G>T (p.Gly146Val)	Osteogenesis imperfecta type 15 [RCV004723405]\|not provided [RCV003682056]	likely pathogenic\|uncertain significance	12	48980502	48980502	Human	1	name , alternate_id
404979384	CV3009567	single nucleotide variant	NM_005430.4(WNT1):c.746G>T (p.Arg249Leu)	not provided [RCV003690976]	uncertain significance	12	48981273	48981273	Human		name
405038625	CV3013503	single nucleotide variant	NM_005430.4(WNT1):c.953C>A (p.Ser318Ter)	not provided [RCV003696148]	pathogenic	12	48981480	48981480	Human		name
405245390	CV3051486	single nucleotide variant	NM_005430.4(WNT1):c.784G>A (p.Gly262Ser)	not provided [RCV003720284]	uncertain significance	12	48981311	48981311	Human		name
405117726	CV3116005	single nucleotide variant	NM_005430.4(WNT1):c.881A>T (p.Lys294Ile)	not provided [RCV003814495]	uncertain significance	12	48981408	48981408	Human		name
405128708	CV3133209	single nucleotide variant	NM_005430.4(WNT1):c.721G>T (p.Ala241Ser)	not provided [RCV003838179]	uncertain significance	12	48981248	48981248	Human		name
405223518	CV3151167	single nucleotide variant	NM_005430.4(WNT1):c.643C>G (p.Arg215Gly)	not provided [RCV003847592]	uncertain significance	12	48981170	48981170	Human		name
405177119	CV3152327	single nucleotide variant	NM_005430.4(WNT1):c.545G>A (p.Arg182Gln)	not provided [RCV003858282]	uncertain significance	12	48980610	48980610	Human		name
405213993	CV3169970	single nucleotide variant	NM_005430.4(WNT1):c.350T>G (p.Val117Gly)	not provided [RCV003862575]	uncertain significance	12	48979713	48979713	Human		name
402466322	CV3173628	single nucleotide variant	NM_005430.4(WNT1):c.899C>T (p.Thr300Met)	not provided [RCV003873102]	uncertain significance	12	48981426	48981426	Human		name
405812085	CV3352905	single nucleotide variant	NM_005430.4(WNT1):c.623C>T (p.Thr208Met)	Inborn genetic diseases [RCV004483105]	uncertain significance	12	48980688	48980688	Human	1	name
405812087	CV3352906	single nucleotide variant	NM_005430.4(WNT1):c.818G>T (p.Arg273Leu)	Inborn genetic diseases [RCV004483106]	uncertain significance	12	48981345	48981345	Human	1	name
407427125	CV3410462	single nucleotide variant	NM_005430.4(WNT1):c.780C>A (p.Asn260Lys)	not specified [RCV004586109]	uncertain significance	12	48981307	48981307	Human		name
407476026	CV3494830	single nucleotide variant	NM_005430.4(WNT1):c.397G>A (p.Ala133Thr)	Osteogenesis imperfecta [RCV004690731]\|Osteogenesis imperfecta type 15 [RCV005006489]	likely pathogenic	12	48980462	48980462	Human	2	name , alternate_id
408393977	CV3521658	single nucleotide variant	NM_005430.4(WNT1):c.437G>A (p.Gly146Asp)	Osteogenesis imperfecta type 15 [RCV004764456]	likely pathogenic	12	48980502	48980502	Human	1	name , alternate_id
408394338	CV3521955	single nucleotide variant	NM_005430.4(WNT1):c.750C>G (p.Phe250Leu)	Osteogenesis imperfecta type 15 [RCV004764754]	uncertain significance	12	48981277	48981277	Human	1	name , alternate_id
408388986	CV3522845	single nucleotide variant	NM_005430.4(WNT1):c.761C>A (p.Ser254Ter)	not provided [RCV004769226]	likely pathogenic	12	48981288	48981288	Human		name
408383140	CV3525757	single nucleotide variant	NM_005430.4(WNT1):c.620G>C (p.Arg207Pro)	not specified [RCV004766667]	uncertain significance	12	48980685	48980685	Human		name
596921999	CV3535628	single nucleotide variant	NM_005430.4(WNT1):c.589C>A (p.Leu197Ile)	Osteogenesis imperfecta type 15 [RCV004785183]\|not provided [RCV005105057]	uncertain significance	12	48980654	48980654	Human	1	name , alternate_id
597631041	CV3624187	single nucleotide variant	NM_005430.4(WNT1):c.488C>G (p.Pro163Arg)	Inborn genetic diseases [RCV004967495]	uncertain significance	12	48980553	48980553	Human	1	name
12842045	CV372326	single nucleotide variant	NM_005430.4(WNT1):c.521T>C (p.Ile174Thr)	Osteogenesis imperfecta type 15 [RCV005252893]\|not provided [RCV000433696]	uncertain significance	12	48980586	48980586	Human	1	name , alternate_id
597897988	CV3740773	single nucleotide variant	NM_005430.4(WNT1):c.365G>A (p.Arg122Gln)	not provided [RCV005071936]	uncertain significance	12	48980430	48980430	Human		name
597912342	CV3745592	single nucleotide variant	NM_005430.4(WNT1):c.574C>T (p.Arg192Trp)	not provided [RCV005073593]	uncertain significance	12	48980639	48980639	Human		name
597849613	CV3746718	single nucleotide variant	NM_005430.4(WNT1):c.466C>G (p.Arg156Gly)	not provided [RCV005066115]	uncertain significance	12	48980531	48980531	Human		name
597935595	CV3759446	single nucleotide variant	NM_005430.4(WNT1):c.639G>T (p.Glu213Asp)	not provided [RCV005076566]	uncertain significance	12	48981166	48981166	Human		name
597918634	CV3768517	single nucleotide variant	NM_005430.4(WNT1):c.451T>C (p.Cys151Arg)	not provided [RCV005114880]	uncertain significance	12	48980516	48980516	Human		name
597906513	CV3773087	single nucleotide variant	NM_005430.4(WNT1):c.388A>G (p.Ile130Val)	not provided [RCV005113151]	uncertain significance	12	48980453	48980453	Human		name
597935191	CV3793708	single nucleotide variant	NM_005430.4(WNT1):c.500G>T (p.Trp167Leu)	not provided [RCV005132364]	uncertain significance	12	48980565	48980565	Human		name
597935199	CV3793709	single nucleotide variant	NM_005430.4(WNT1):c.475G>T (p.Gly159Cys)	not provided [RCV005132365]	uncertain significance	12	48980540	48980540	Human		name
597954352	CV3795762	single nucleotide variant	NM_005430.4(WNT1):c.553G>C (p.Val185Leu)	not provided [RCV005136772]	uncertain significance	12	48980618	48980618	Human		name
597871467	CV3806010	single nucleotide variant	NM_005430.4(WNT1):c.578A>T (p.Asp193Val)	not provided [RCV005148420]	uncertain significance	12	48980643	48980643	Human		name
597861225	CV3822484	single nucleotide variant	NM_005430.4(WNT1):c.854C>G (p.Ser285Cys)	not provided [RCV005175014]	uncertain significance	12	48981381	48981381	Human		name
597931733	CV3827144	single nucleotide variant	NM_005430.4(WNT1):c.854C>T (p.Ser285Phe)	not provided [RCV005157157]	uncertain significance	12	48981381	48981381	Human		name
597943965	CV3847804	single nucleotide variant	NM_005430.4(WNT1):c.932C>T (p.Ala311Val)	not provided [RCV005188532]	uncertain significance	12	48981459	48981459	Human		name
597906942	CV3853504	single nucleotide variant	NM_005430.4(WNT1):c.990C>A (p.Cys330Ter)	not provided [RCV005202983]	pathogenic	12	48981517	48981517	Human		name
598199835	CV3892592	single nucleotide variant	NM_005430.4(WNT1):c.745C>G (p.Arg249Gly)	not provided [RCV005254425]	uncertain significance	12	48981272	48981272	Human		name
13509029	CV482021	single nucleotide variant	NM_005430.4(WNT1):c.364C>T (p.Arg122Ter)	not provided [RCV000578793]	pathogenic	12	48980429	48980429	Human		name
8611922	CV59406	single nucleotide variant	NM_005430.4(WNT1):c.565G>T (p.Glu189Ter)	Osteogenesis imperfecta type 15 [RCV000043494]	pathogenic	12	48980630	48980630	Human	1	name , alternate_id
8611923	CV59407	single nucleotide variant	NM_005430.4(WNT1):c.884C>A (p.Ser295Ter)	Inborn genetic diseases [RCV001267401]\|Osteogenesis imperfecta type 15 [RCV000043495]\|Osteogenesis imperfecta type 15 [RCV005007964]\|not provided [RCV000489304]	pathogenic\|likely pathogenic	12	48981411	48981411	Human	2	name , alternate_id
8611926	CV59410	single nucleotide variant	NM_005430.4(WNT1):c.703C>T (p.Arg235Trp)	OSTEOPOROSIS, EARLY-ONSET, SUSCEPTIBILITY TO [RCV000043498]	risk factor	12	48981230	48981230	Human	1	name
14692851	CV615942	single nucleotide variant	NM_005430.4(WNT1):c.754G>C (p.Gly252Arg)	Inborn genetic diseases [RCV002533979]\|Osteogenesis imperfecta [RCV000770973]\|not provided [RCV001585697]\|not specified [RCV003330945]	uncertain significance	12	48981281	48981281	Human	2	name
14692852	CV615943	single nucleotide variant	NM_005430.4(WNT1):c.989G>A (p.Cys330Tyr)	Osteogenesis imperfecta [RCV000770974]	uncertain significance	12	48981516	48981516	Human	1	name
8611988	CV65585	single nucleotide variant	NM_005430.4(WNT1):c.652T>G (p.Cys218Gly)	OSTEOPOROSIS, EARLY-ONSET, SUSCEPTIBILITY TO [RCV000043638]	risk factor	12	48981179	48981179	Human	1	name
15166984	CV672343	single nucleotide variant	NM_005430.4(WNT1):c.501G>C (p.Trp167Cys)	Osteogenesis imperfecta type III [RCV000860011]\|not provided [RCV002538348]	pathogenic\|likely pathogenic\|uncertain significance	12	48980566	48980566	Human	1	name
21074267	CV796778	single nucleotide variant	NM_005430.4(WNT1):c.664G>C (p.Gly222Arg)	not provided [RCV000994911]	likely pathogenic	12	48981191	48981191	Human		name
40816245	CV858279	single nucleotide variant	NM_005430.4(WNT1):c.937C>A (p.Arg313Ser)	Osteogenesis imperfecta [RCV001260284]	uncertain significance	12	48981464	48981464	Human	1	name
28877591	CV861573	deletion	NM_005430.4(WNT1):c.1060del (p.His354fs)	Osteogenesis imperfecta type 15 [RCV001095660]	uncertain significance	12	48981586	48981586	Human	1	name , alternate_id
150423093	CV1181009	single nucleotide variant	NM_005430.4(WNT1):c.1007C>T (p.Thr336Met)	Osteogenesis imperfecta [RCV002276781]\|not provided [RCV001553544]	benign\|likely benign\|uncertain significance	12	48981534	48981534	Human	1	name
151828806	CV1348333	single nucleotide variant	NM_005430.4(WNT1):c.1064T>C (p.Val355Ala)	not provided [RCV001870329]	uncertain significance	12	48981591	48981591	Human		name
151859299	CV1389593	single nucleotide variant	NM_005430.4(WNT1):c.1037A>C (p.Asn346Thr)	not provided [RCV001905078]	uncertain significance	12	48981564	48981564	Human		name
151827851	CV1465308	single nucleotide variant	NM_005430.4(WNT1):c.1061A>T (p.His354Leu)	not provided [RCV002014012]	uncertain significance	12	48981588	48981588	Human		name
156273981	CV1900104	single nucleotide variant	NM_005430.4(WNT1):c.1093G>A (p.Val365Ile)	not provided [RCV003086885]	uncertain significance	12	48981620	48981620	Human		name
156404741	CV1916706	single nucleotide variant	NM_005430.4(WNT1):c.1027G>C (p.Glu343Gln)	not provided [RCV002606168]	uncertain significance	12	48981554	48981554	Human		name
156300391	CV1955531	single nucleotide variant	NM_005430.4(WNT1):c.1030C>A (p.Arg344Ser)	not provided [RCV002578202]	uncertain significance	12	48981557	48981557	Human		name
156217685	CV2172991	single nucleotide variant	NM_005430.4(WNT1):c.1064T>G (p.Val355Gly)	not provided [RCV003025067]	uncertain significance	12	48981591	48981591	Human		name
156081910	CV2184223	single nucleotide variant	NM_005430.4(WNT1):c.1105T>G (p.Cys369Gly)	not provided [RCV003054058]	uncertain significance	12	48981632	48981632	Human		name
401739133	CV2738487	single nucleotide variant	NM_005430.4(WNT1):c.1108C>G (p.Leu370Val)	not provided [RCV003575075]\|not specified [RCV003317879]	uncertain significance	12	48981635	48981635	Human		name
405007923	CV2853189	single nucleotide variant	NM_005430.4(WNT1):c.1059C>G (p.Cys353Trp)	not specified [RCV003494383]	uncertain significance	12	48981586	48981586	Human		name
405122232	CV2954070	single nucleotide variant	NM_005430.4(WNT1):c.1025C>G (p.Thr342Ser)	not provided [RCV003667542]	uncertain significance	12	48981552	48981552	Human		name
402502731	CV3006996	single nucleotide variant	NM_005430.4(WNT1):c.1079G>T (p.Cys360Phe)	not provided [RCV003688668]	uncertain significance	12	48981606	48981606	Human		name
405157248	CV3065085	single nucleotide variant	NM_005430.4(WNT1):c.1073G>A (p.Arg358His)	Inborn genetic diseases [RCV004968430]\|not provided [RCV003726847]	uncertain significance	12	48981600	48981600	Human	1	name
405156609	CV3163504	single nucleotide variant	NM_005430.4(WNT1):c.1013C>T (p.Thr338Met)	not provided [RCV003856750]	uncertain significance	12	48981540	48981540	Human		name
407524776	CV3487958	single nucleotide variant	NM_005430.4(WNT1):c.1018C>A (p.Arg340Ser)	Inborn genetic diseases [RCV004678552]	uncertain significance	12	48981545	48981545	Human	1	name
12834201	CV375161	single nucleotide variant	NM_005430.4(WNT1):c.1051T>G (p.Trp351Gly)	not provided [RCV000419959]	uncertain significance	12	48981578	48981578	Human		name
597969680	CV3831988	single nucleotide variant	NM_005430.4(WNT1):c.1035C>A (p.Cys345Ter)	not provided [RCV005166244]	pathogenic	12	48981562	48981562	Human		name
597883134	CV3834136	single nucleotide variant	NM_005430.4(WNT1):c.1101C>A (p.His367Gln)	not provided [RCV005178455]	uncertain significance	12	48981628	48981628	Human		name
598202652	CV3892808	single nucleotide variant	NM_005430.4(WNT1):c.1006A>C (p.Thr336Pro)	not provided [RCV005255137]	uncertain significance	12	48981533	48981533	Human		name
598275505	CV3937148	single nucleotide variant	NM_005430.4(WNT1):c.1076A>G (p.Asn359Ser)	Inborn genetic diseases [RCV005304639]	uncertain significance	12	48981603	48981603	Human	1	name
13831411	CV583117	single nucleotide variant	NM_005430.4(WNT1):c.1090C>G (p.Arg364Gly)	Osteogenesis imperfecta type 15 [RCV000723329]	uncertain significance	12	48981617	48981617	Human	1	name , alternate_id
8611925	CV59409	single nucleotide variant	NM_005430.4(WNT1):c.1063G>T (p.Val355Phe)	Keratoconus [RCV000678662]\|Osteogenesis imperfecta type 15 [RCV000043497]	pathogenic\|uncertain significance	12	48981590	48981590	Human	3	name , alternate_id
151720156	CV1481322	deletion	NM_005430.4(WNT1):c.287_300del (p.Gln96fs)	not provided [RCV001982945]	pathogenic	12	48979648	48979661	Human		name
151883451	CV1476576	deletion	NM_005430.4(WNT1):c.479_480del (p.Pro160fs)	not provided [RCV001886943]	pathogenic	12	48980542	48980543	Human		name
156045321	CV1999215	indel	NM_005430.4(WNT1):c.5_6delinsAA (p.Gly2Glu)	not provided [RCV002659186]	uncertain significance	12	48978655	48978656	Human		name
8611924	CV59408	duplication	NM_005430.4(WNT1):c.946_949dup (p.Ser317fs)	Osteogenesis imperfecta type 15 [RCV000043496]	pathogenic	12	48981472	48981473	Human	1	name , alternate_id
153349937	CV1693589	deletion	NM_005430.4(WNT1):c.999_1021del (p.Thr336fs)	not provided [RCV002276373]	pathogenic\|likely pathogenic	12	48981525	48981547	Human		name
151823316	CV1415269	deletion	NM_005430.4(WNT1):c.1005_1027del (p.Thr336fs)	not provided [RCV001954978]	pathogenic\|uncertain significance	12	48981527	48981549	Human		name
11649219	CV284770	single nucleotide variant	NM_025216.3(WNT10A):c.*15C>T	Odonto-onycho-dermal dysplasia [RCV000285858]\|SchC6pf-Schulz-Passarge syndrome [RCV000406243]\|Tooth agenesis, selective, 4 [RCV000339827]	uncertain significance	2	218893286	218893286	Human	3	name
28901307	CV883762	single nucleotide variant	NM_025216.3(WNT10A):c.-70G>C	Odonto-onycho-dermal dysplasia [RCV001143122]\|SchC6pf-Schulz-Passarge syndrome [RCV001143124]\|Tooth agenesis, selective, 4 [RCV001143123]	uncertain significance	2	218880926	218880926	Human	3	name
150462028	CV1214586	single nucleotide variant	NM_003394.4(WNT10B):c.*185A>G	not provided [RCV001613579]	benign	12	48965910	48965910	Human		name
11584659	CV284729	single nucleotide variant	NM_025216.2(WNT10A):c.-341A>G	Odonto-onycho-dermal dysplasia [RCV000367457]\|SchC6pf-Schulz-Passarge syndrome [RCV000275208]\|Selective tooth agenesis [RCV000327931]	uncertain significance	2	218880655	218880655	Human	4	name
11649470	CV284732	single nucleotide variant	NM_025216.2(WNT10A):c.-285C>T	Odonto-onycho-dermal dysplasia [RCV000340050]\|SchC6pf-Schulz-Passarge syndrome [RCV000379484]\|Selective tooth agenesis [RCV000287393]	uncertain significance	2	218880711	218880711	Human	4	name
11589796	CV284737	single nucleotide variant	NM_025216.2(WNT10A):c.-249G>C	Odonto-onycho-dermal dysplasia [RCV000351817]\|Odonto-onycho-dermal dysplasia [RCV002488717]\|SchC6pf-Schulz-Passarge syndrome [RCV000393205]\|Selective tooth agenesis [RCV000313367]	uncertain significance	2	218880747	218880747	Human	5	name
11653708	CV284740	duplication	NM_025216.2(WNT10A):c.-203dup	Odonto-onycho-dermal dysplasia [RCV000312263]\|SchC6pf-Schulz-Passarge syndrome [RCV000364629]\|Selective tooth agenesis [RCV000393221]	likely benign	2	218880787	218880788	Human	4	name
11649084	CV285403	single nucleotide variant	NM_025216.2(WNT10A):c.-433C>G	Odonto-onycho-dermal dysplasia [RCV000343676]\|SchC6pf-Schulz-Passarge syndrome [RCV000381861]\|Selective tooth agenesis [RCV000285189]	uncertain significance	2	218880563	218880563	Human	4	name
11653524	CV285427	single nucleotide variant	NM_025216.3(WNT10A):c.*115C>T	Odonto-onycho-dermal dysplasia [RCV000311654]\|SchC6pf-Schulz-Passarge syndrome [RCV000355840]\|Tooth agenesis, selective, 4 [RCV000395878]	uncertain significance	2	218893386	218893386	Human	3	name
11586249	CV285428	single nucleotide variant	NM_025216.3(WNT10A):c.*431C>T	Odonto-onycho-dermal dysplasia [RCV000378404]\|SchC6pf-Schulz-Passarge syndrome [RCV000286731]\|Tooth agenesis, selective, 4 [RCV000334738]\|not provided [RCV004710877]	benign\|likely benign	2	218893702	218893702	Human	3	name
11588441	CV287631	single nucleotide variant	NM_025216.2(WNT10A):c.-400T>G	Odonto-onycho-dermal dysplasia [RCV000396361]\|SchC6pf-Schulz-Passarge syndrome [RCV000302946]\|Selective tooth agenesis [RCV000342611]	likely benign	2	218880596	218880596	Human	4	name
11583879	CV287632	single nucleotide variant	NM_025216.2(WNT10A):c.-312C>T	Odonto-onycho-dermal dysplasia [RCV000327152]\|SchC6pf-Schulz-Passarge syndrome [RCV000269728]\|Selective tooth agenesis [RCV000385171]	likely benign	2	218880684	218880684	Human	4	name
11648500	CV287635	single nucleotide variant	NM_025216.2(WNT10A):c.-149G>T	Odonto-onycho-dermal dysplasia [RCV000318400]\|SchC6pf-Schulz-Passarge syndrome [RCV000386984]\|Selective tooth agenesis [RCV000282018]\|not provided [RCV004694530]	uncertain significance	2	218880847	218880847	Human	4	name
11587919	CV287638	single nucleotide variant	NM_025216.3(WNT10A):c.*108G>A	Odonto-onycho-dermal dysplasia [RCV000343286]\|SchC6pf-Schulz-Passarge syndrome [RCV000395886]\|Tooth agenesis, selective, 4 [RCV000298619]	likely benign\|uncertain significance	2	218893379	218893379	Human	3	name
11584763	CV287639	single nucleotide variant	NM_025216.3(WNT10A):c.*128T>C	Odonto-onycho-dermal dysplasia [RCV000276113]\|SchC6pf-Schulz-Passarge syndrome [RCV000333400]\|Tooth agenesis, selective, 4 [RCV000368319]	likely benign	2	218893399	218893399	Human	3	name
11583985	CV287640	single nucleotide variant	NM_025216.3(WNT10A):c.*216G>C	Odonto-onycho-dermal dysplasia [RCV000362436]\|SchC6pf-Schulz-Passarge syndrome [RCV000270312]\|Tooth agenesis, selective, 4 [RCV000327725]	likely benign	2	218893487	218893487	Human	3	name
11585755	CV287641	single nucleotide variant	NM_025216.3(WNT10A):c.*275C>T	Odonto-onycho-dermal dysplasia [RCV000283268]\|SchC6pf-Schulz-Passarge syndrome [RCV000321420]\|Tooth agenesis, selective, 4 [RCV000384690]	likely benign	2	218893546	218893546	Human	3	name
11648252	CV287652	single nucleotide variant	NM_025216.3(WNT10A):c.*441C>T	Odonto-onycho-dermal dysplasia [RCV000280798]\|SchC6pf-Schulz-Passarge syndrome [RCV000372959]\|Tooth agenesis, selective, 4 [RCV000338084]	uncertain significance	2	218893712	218893712	Human	3	name
11651245	CV287862	single nucleotide variant	NM_025216.2(WNT10A):c.-370C>A	Odonto-onycho-dermal dysplasia [RCV000297679]\|SchC6pf-Schulz-Passarge syndrome [RCV000399839]\|Selective tooth agenesis [RCV000336880]	uncertain significance	2	218880626	218880626	Human	4	name
11647463	CV287863	single nucleotide variant	NM_025216.2(WNT10A):c.-358G>A	Odonto-onycho-dermal dysplasia [RCV000354814]\|SchC6pf-Schulz-Passarge syndrome [RCV000315106]\|Selective tooth agenesis [RCV000276465]	uncertain significance	2	218880638	218880638	Human	4	name
11585509	CV287865	single nucleotide variant	NM_025216.2(WNT10A):c.-270G>C	Odonto-onycho-dermal dysplasia [RCV000281436]\|SchC6pf-Schulz-Passarge syndrome [RCV000334363]\|Selective tooth agenesis [RCV000378266]	uncertain significance	2	218880726	218880726	Human	4	name
11653399	CV287866	single nucleotide variant	NM_025216.2(WNT10A):c.-202G>C	Odonto-onycho-dermal dysplasia [RCV000365189]\|SchC6pf-Schulz-Passarge syndrome [RCV000310576]\|Selective tooth agenesis [RCV000390295]	uncertain significance	2	218880794	218880794	Human	4	name
11645540	CV287872	duplication	NM_025216.2(WNT10A):c.-194dup	Odonto-onycho-dermal dysplasia [RCV000321025]\|SchC6pf-Schulz-Passarge syndrome [RCV000265874]\|Selective tooth agenesis [RCV000361608]	uncertain significance	2	218880794	218880795	Human	4	name
11645735	CV287873	single nucleotide variant	NM_025216.2(WNT10A):c.-153G>A	Odonto-onycho-dermal dysplasia [RCV000266900]\|SchC6pf-Schulz-Passarge syndrome [RCV000372076]\|Selective tooth agenesis [RCV000317473]	uncertain significance	2	218880843	218880843	Human	4	name
28896543	CV883761	single nucleotide variant	NM_025216.3(WNT10A):c.-123C>A	Odonto-onycho-dermal dysplasia [RCV001143120]\|Odonto-onycho-dermal dysplasia [RCV002482269]\|SchC6pf-Schulz-Passarge syndrome [RCV001141276]\|Tooth agenesis, selective, 4 [RCV001143121]	uncertain significance	2	218880873	218880873	Human	3	name
28891024	CV883775	single nucleotide variant	NM_025216.3(WNT10A):c.*139C>G	Odonto-onycho-dermal dysplasia [RCV001139236]\|SchC6pf-Schulz-Passarge syndrome [RCV001139235]\|Tooth agenesis, selective, 4 [RCV001139234]	uncertain significance	2	218893410	218893410	Human	3	name
28898136	CV883776	single nucleotide variant	NM_025216.3(WNT10A):c.*238C>T	Odonto-onycho-dermal dysplasia [RCV001141850]\|SchC6pf-Schulz-Passarge syndrome [RCV001141851]\|Tooth agenesis, selective, 4 [RCV001141849]	uncertain significance	2	218893509	218893509	Human	3	name
28898141	CV883777	single nucleotide variant	NM_025216.3(WNT10A):c.*339C>T	Odonto-onycho-dermal dysplasia [RCV001143649]\|SchC6pf-Schulz-Passarge syndrome [RCV001141852]\|Tooth agenesis, selective, 4 [RCV001141853]	uncertain significance	2	218893610	218893610	Human	3	name
127294118	CV1133230	single nucleotide variant	NM_025216.3(WNT10A):c.756+7G>A	Odonto-onycho-dermal dysplasia [RCV001496914]	likely benign	2	218890370	218890370	Human	1	name
127331143	CV1133231	single nucleotide variant	NM_025216.3(WNT10A):c.757-6C>T	Odonto-onycho-dermal dysplasia [RCV001488623]	likely benign	2	218892768	218892768	Human	1	name
152037621	CV1576381	single nucleotide variant	NM_025216.3(WNT10A):c.113+8C>A	Odonto-onycho-dermal dysplasia [RCV002107255]	likely benign	2	218881116	218881116	Human	1	name
152137155	CV1625476	single nucleotide variant	NM_025216.3(WNT10A):c.376+9C>T	Odonto-onycho-dermal dysplasia [RCV002137696]	likely benign	2	218882432	218882432	Human	1	name
152122158	CV1640885	single nucleotide variant	NM_025216.3(WNT10A):c.756+9C>A	Odonto-onycho-dermal dysplasia [RCV002098304]	likely benign	2	218890372	218890372	Human	1	name
155904832	CV2007270	single nucleotide variant	NM_025216.3(WNT10A):c.113+1G>A	Odonto-onycho-dermal dysplasia [RCV002681329]	likely pathogenic	2	218881109	218881109	Human	1	name
156147665	CV2090956	single nucleotide variant	NM_025216.3(WNT10A):c.757-9C>A	Odonto-onycho-dermal dysplasia [RCV002890543]	likely benign	2	218892765	218892765	Human	1	name
402521213	CV3091995	single nucleotide variant	NM_025216.3(WNT10A):c.114-8G>A	Odonto-onycho-dermal dysplasia [RCV003790441]	likely benign	2	218882153	218882153	Human	1	name
405004554	CV3095954	single nucleotide variant	NM_025216.3(WNT10A):c.376+8C>T	Odonto-onycho-dermal dysplasia [RCV003794104]	likely benign	2	218882431	218882431	Human	1	name
405003302	CV3102156	single nucleotide variant	NM_025216.3(WNT10A):c.113+7C>A	Odonto-onycho-dermal dysplasia [RCV003804202]	likely benign	2	218881115	218881115	Human	1	name
597879187	CV3813790	single nucleotide variant	NM_003394.4(WNT10B):c.74+16T>C	not provided [RCV005149532]	likely benign	12	48970440	48970440	Human		name
597910471	CV3879397	single nucleotide variant	NM_025216.3(WNT10A):c.113+3G>A	Odonto-onycho-dermal dysplasia [RCV005221797]	uncertain significance	2	218881111	218881111	Human	1	name
13609118	CV535382	single nucleotide variant	NM_003394.4(WNT10B):c.338-1G>C	Split hand-foot malformation 6 [RCV000656339]	pathogenic\|likely pathogenic	12	48968320	48968320	Human	1	name
15164676	CV730869	single nucleotide variant	NM_003394.4(WNT10B):c.337+7C>T	not provided [RCV000882249]	likely benign	12	48970082	48970082	Human		name
34888586	CV917809	single nucleotide variant	NM_025216.3(WNT10A):c.756+1G>A	Odonto-onycho-dermal dysplasia [RCV001194666]	pathogenic	2	218890364	218890364	Human	1	name
38478658	CV939877	single nucleotide variant	NM_025216.3(WNT10A):c.376+1G>A	Odonto-onycho-dermal dysplasia [RCV001205643]\|Odonto-onycho-dermal dysplasia [RCV003329173]\|SchC6pf-Schulz-Passarge syndrome [RCV001828648]\|not provided [RCV001780113]	pathogenic\|likely pathogenic	2	218882424	218882424	Human	3	name
150442637	CV1249150	single nucleotide variant	NM_025216.3(WNT10A):c.114-56T>C	not provided [RCV001666582]	benign	2	218882105	218882105	Human		name
150459358	CV1268331	single nucleotide variant	NM_003394.4(WNT10B):c.-40-39C>T	not provided [RCV001693328]	benign	12	48970608	48970608	Human		name
8653202	CV129777	single nucleotide variant	NM_004626.2(WNT11):c.83+2925G>T	Lung cancer [RCV000110264]	uncertain significance	11	76203400	76203400	Human		name
152042419	CV1670001	single nucleotide variant	NM_003394.4(WNT10B):c.337+14G>C	not provided [RCV002224903]	uncertain significance	12	48970075	48970075	Human		name
156350537	CV1965381	single nucleotide variant	NM_025216.3(WNT10A):c.114-10A>T	Odonto-onycho-dermal dysplasia [RCV002581026]	likely benign	2	218882151	218882151	Human	1	name
11579732	CV284763	single nucleotide variant	NM_025216.3(WNT10A):c.756+13C>A	Odonto-onycho-dermal dysplasia [RCV000394128]\|Odonto-onycho-dermal dysplasia [RCV003765945]\|SchC6pf-Schulz-Passarge syndrome [RCV000352056]\|Tooth agenesis, selective, 4 [RCV000311299]	likely benign\|uncertain significance	2	218890376	218890376	Human	3	name
11579601	CV284764	single nucleotide variant	NM_025216.3(WNT10A):c.756+14C>T	Odonto-onycho-dermal dysplasia [RCV000394115]\|Odonto-onycho-dermal dysplasia [RCV002523114]\|SchC6pf-Schulz-Passarge syndrome [RCV000307935]\|Tooth agenesis, selective, 4 [RCV000362680]	benign\|likely benign\|uncertain significance	2	218890377	218890377	Human	3	name
404990796	CV3084228	single nucleotide variant	NM_025216.3(WNT10A):c.376+17C>A	Odonto-onycho-dermal dysplasia [RCV003782421]	likely benign	2	218882440	218882440	Human	1	name
405052423	CV3084777	single nucleotide variant	NM_025216.3(WNT10A):c.757-17G>T	Odonto-onycho-dermal dysplasia [RCV003798184]	likely benign	2	218892757	218892757	Human	1	name
405020711	CV3085553	single nucleotide variant	NM_025216.3(WNT10A):c.113+10C>T	Odonto-onycho-dermal dysplasia [RCV003785276]	likely benign	2	218881118	218881118	Human	1	name
402510931	CV3087126	single nucleotide variant	NM_025216.3(WNT10A):c.757-20C>A	Odonto-onycho-dermal dysplasia [RCV003789637]	likely benign	2	218892754	218892754	Human	1	name
402500776	CV3089631	single nucleotide variant	NM_025216.3(WNT10A):c.756+17T>C	Odonto-onycho-dermal dysplasia [RCV003788554]	likely benign	2	218890380	218890380	Human	1	name
402500836	CV3089637	single nucleotide variant	NM_025216.3(WNT10A):c.113+17T>C	Odonto-onycho-dermal dysplasia [RCV003788560]	likely benign	2	218881125	218881125	Human	1	name
402505327	CV3090259	single nucleotide variant	NM_025216.3(WNT10A):c.113+19C>T	Odonto-onycho-dermal dysplasia [RCV003789027]	likely benign	2	218881127	218881127	Human	1	name
402487312	CV3090501	single nucleotide variant	NM_025216.3(WNT10A):c.114-10A>G	Odonto-onycho-dermal dysplasia [RCV003787162]	likely benign	2	218882151	218882151	Human	1	name
402489126	CV3090871	single nucleotide variant	NM_025216.3(WNT10A):c.376+18C>A	Odonto-onycho-dermal dysplasia [RCV003787373]	likely benign	2	218882441	218882441	Human	1	name
402521501	CV3092019	single nucleotide variant	NM_025216.3(WNT10A):c.756+18G>A	Odonto-onycho-dermal dysplasia [RCV003790465]	likely benign	2	218890381	218890381	Human	1	name
402482499	CV3093243	single nucleotide variant	NM_025216.3(WNT10A):c.756+20G>A	Odonto-onycho-dermal dysplasia [RCV003786594]	likely benign	2	218890383	218890383	Human	1	name
405001100	CV3099303	deletion	NM_025216.3(WNT10A):c.756+17del	Odonto-onycho-dermal dysplasia [RCV003793724]	likely benign	2	218890380	218890380	Human	1	name
402524950	CV3102631	single nucleotide variant	NM_025216.3(WNT10A):c.377-18C>G	Odonto-onycho-dermal dysplasia [RCV003790725]	likely benign	2	218889966	218889966	Human	1	name
402525185	CV3102648	single nucleotide variant	NM_025216.3(WNT10A):c.756+15C>A	Odonto-onycho-dermal dysplasia [RCV003790742]	likely benign	2	218890378	218890378	Human	1	name
405129153	CV3110869	single nucleotide variant	NM_025216.3(WNT10A):c.757-16G>A	Odonto-onycho-dermal dysplasia [RCV003815748]	likely benign	2	218892758	218892758	Human	1	name
405107279	CV3113791	single nucleotide variant	NM_025216.3(WNT10A):c.376+19T>C	Odonto-onycho-dermal dysplasia [RCV003812914]	likely benign	2	218882442	218882442	Human	1	name
597848090	CV3736815	single nucleotide variant	NM_003394.4(WNT10B):c.712-20T>G	not provided [RCV005065974]	likely benign	12	48966573	48966573	Human		name
597927304	CV3855490	single nucleotide variant	NM_003394.4(WNT10B):c.337+19G>T	not provided [RCV005206089]	likely benign	12	48970070	48970070	Human		name
597883485	CV3866007	single nucleotide variant	NM_025216.3(WNT10A):c.756+14C>A	Odonto-onycho-dermal dysplasia [RCV005217672]	likely benign	2	218890377	218890377	Human	1	name
597865796	CV3868842	single nucleotide variant	NM_025216.3(WNT10A):c.376+17C>G	Odonto-onycho-dermal dysplasia [RCV005214962]	likely benign	2	218882440	218882440	Human	1	name
28896853	CV887275	single nucleotide variant	NM_025216.3(WNT10A):c.377-11T>C	Odonto-onycho-dermal dysplasia [RCV001141385]\|Odonto-onycho-dermal dysplasia [RCV003769674]\|SchC6pf-Schulz-Passarge syndrome [RCV001141384]\|Tooth agenesis, selective, 4 [RCV001141386]	likely benign\|uncertain significance	2	218889973	218889973	Human	3	name
150410172	CV1191421	single nucleotide variant	NM_003394.4(WNT10B):c.712-292A>G	not provided [RCV001565914]	likely benign	12	48966845	48966845	Human		name
151351465	CV1323469	single nucleotide variant	NM_000158.4(GBE1):c.1843G>C (p.Ala615Pro)	Osteogenesis imperfecta type 15 [RCV001806325]	likely pathogenic	3	81535286	81535286	Human	1	alternate_id
405243351	CV2974864	microsatellite	NM_003394.4(WNT10B):c.75-12_75-10del	not provided [RCV003684506]	uncertain significance	12	48970361	48970363	Human		name
402486300	CV3093733	deletion	NM_025216.3(WNT10A):c.377-12_377-10del	Odonto-onycho-dermal dysplasia [RCV003786934]	likely benign	2	218889971	218889973	Human	1	name
405055973	CV3107915	insertion	NM_025216.3(WNT10A):c.376+13_376+14insCTTTCTTTCCAAGTTATGGATGTCCATTGTGTGGGGTCAGGTGACCTCCGTTTCCTCCA	Odonto-onycho-dermal dysplasia [RCV003808661]	likely benign	2	218882436	218882437	Human	1	name
405267338	CV3202206	single nucleotide variant	NM_004626.3(WNT11):c.339C>T (p.Phe113=)	WNT11-related disorder [RCV003911675]	likely benign	11	76194825	76194825	Human		name , trait , alternate_id
405294848	CV3209262	single nucleotide variant	NM_004626.3(WNT11):c.198G>A (p.Met66Ile)	Bladder exstrophy-epispadias-cloacal extrophy complex [RCV004556104]\|WNT11-related disorder [RCV003934766]	benign\|likely benign	11	76196604	76196604	Human	1	name , alternate_id
127237178	CV1069103	single nucleotide variant	NM_025216.3(WNT10A):c.636C>T (p.Gly212=)	Odonto-onycho-dermal dysplasia [RCV001414842]\|WNT10A-related disorder [RCV004540283]	likely benign	2	218890243	218890243	Human	2	name , alternate_id
127268695	CV1090786	single nucleotide variant	NM_025216.3(WNT10A):c.408C>G (p.Ile136Met)	Odonto-onycho-dermal dysplasia [RCV001430053]\|WNT10A-related disorder [RCV004734185]\|not provided [RCV003229056]	likely benign\|uncertain significance	2	218890015	218890015	Human	2	name , alternate_id
8696091	CV143206	single nucleotide variant	NM_025216.3(WNT10A):c.637G>A (p.Gly213Ser)	Odonto-onycho-dermal dysplasia [RCV000325824]\|Odonto-onycho-dermal dysplasia [RCV000490390]\|SchC6pf-Schulz-Passarge syndrome [RCV000270809]\|Tooth agenesis [RCV000845115]\|Tooth agenesis, selective, 2 [RCV003233110]\|Tooth agenesis, selective, 4 [RCV000128463]\|WNT1 ... (more) 0A-related disorder [RCV004734670]\|not provided [RCV001555273]	pathogenic\|likely pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	218890244	218890244	Human	9	name , alternate_id
8696091	CV143206	single nucleotide variant	NM_025216.3(WNT10A):c.637G>A (p.Gly213Ser)	Odonto-onycho-dermal dysplasia [RCV000325824]\|Odonto-onycho-dermal dysplasia [RCV000490390]\|SchC6pf-Schulz-Passarge syndrome [RCV000270809]\|Tooth agenesis [RCV000845115]\|Tooth agenesis, selective, 2 [RCV003233110]\|Tooth agenesis, selective, 4 [RCV000128463]\|WNT1 ... (more) 0A-related disorder [RCV004734670]\|not provided [RCV001555273]	pathogenic\|likely pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	218890244	218890245	Human	9	name , alternate_id
10046769	CV187237	single nucleotide variant	NM_025216.3(WNT10A):c.487C>T (p.Arg163Trp)	Bladder exstrophy-epispadias-cloacal extrophy complex [RCV000172902]\|Odonto-onycho-dermal dysplasia [RCV001136665]\|Odonto-onycho-dermal dysplasia [RCV001239125]\|SchC6pf-Schulz-Passarge syndrome [RCV001136664]\|WNT10A-related disorder [RCV004535152]\|not provided [ ... (more) RCV000522644]	likely pathogenic\|benign\|uncertain significance	2	218890094	218890094	Human	4	name , alternate_id
8558099	CV19500	single nucleotide variant	NM_025216.3(WNT10A):c.321C>A (p.Cys107Ter)	Ectodermal dysplasia [RCV001729335]\|Inborn genetic diseases [RCV000190800]\|Odonto-onycho-dermal dysplasia [RCV000004715]\|Odonto-onycho-dermal dysplasia [RCV000477935]\|Odonto-onycho-dermal dysplasia [RCV000536747]\|SchC6pf-Schulz-Passarge syndrome [RCV000004716]\|Tooth agenesis, selective, 4 [RCV000030 ... (more) 650]\|WNT10A-related disorder [RCV000779308]\|not provided [RCV000255732]\|not specified [RCV002247247]	pathogenic\|uncertain significance\|not provided	2	218882368	218882368	Human	6	name , alternate_id
8558100	CV19501	single nucleotide variant	NM_025216.3(WNT10A):c.682T>A (p.Phe228Ile)	Ectodermal dysplasia WNT10A related [RCV005249981]\|Ectodermal dysplasia [RCV001729336]\|Hypohidrotic ectodermal dysplasia [RCV000754840]\|Inborn genetic diseases [RCV000622932]\|Odonto-onycho-dermal dysplasia [RCV000004717]\|Odonto-onycho-dermal dysplasia [RCV000550 ... (more) 721]\|Odonto-onycho-dermal dysplasia [RCV001535660]\|SchC6pf-Schulz-Passarge syndrome [RCV001813948]\|See cases [RCV004584315]\|Tooth agenesis [RCV000845113]\|Tooth agenesis, selective, 4 [RCV000445356]\|WNT10A-related disorder [RCV004528071]\|not provided [RCV000255788]	pathogenic\|likely pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|low penetrance\|not provided	2	218890289	218890289	Human	28	name , alternate_id
8558100	CV19501	single nucleotide variant	NM_025216.3(WNT10A):c.682T>A (p.Phe228Ile)	Ectodermal dysplasia WNT10A related [RCV005249981]\|Ectodermal dysplasia [RCV001729336]\|Hypohidrotic ectodermal dysplasia [RCV000754840]\|Inborn genetic diseases [RCV000622932]\|Odonto-onycho-dermal dysplasia [RCV000004717]\|Odonto-onycho-dermal dysplasia [RCV000550 ... (more) 721]\|Odonto-onycho-dermal dysplasia [RCV001535660]\|SchC6pf-Schulz-Passarge syndrome [RCV001813948]\|See cases [RCV004584315]\|Tooth agenesis [RCV000845113]\|Tooth agenesis, selective, 4 [RCV000445356]\|WNT10A-related disorder [RCV004528071]\|not provided [RCV000255788]	pathogenic\|likely pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|low penetrance\|not provided	2	218890289	218890290	Human	28	name , alternate_id
11559905	CV227234	single nucleotide variant	NM_025216.3(WNT10A):c.511C>T (p.Arg171Cys)	Odonto-onycho-dermal dysplasia [RCV000335291]\|Odonto-onycho-dermal dysplasia [RCV000490286]\|Odonto-onycho-dermal dysplasia [RCV005396694]\|SchC6pf-Schulz-Passarge syndrome [RCV000299227]\|Tooth agenesis, selective, 2 [RCV003233498]\|Tooth agenesis, selective, 4 [RCV000396415]\|WNT1 ... (more) 00;'>WNT10A-related disorder [RCV004734859]\|not provided [RCV000255246]	pathogenic\|likely pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	218890118	218890118	Human	4	name , alternate_id
11559731	CV259731	single nucleotide variant	NM_025216.3(WNT10A):c.742C>T (p.Arg248Ter)	Inborn genetic diseases [RCV001266421]\|Odonto-onycho-dermal dysplasia [RCV000677100]\|Odonto-onycho-dermal dysplasia [RCV000823047]\|SchC6pf-Schulz-Passarge syndrome [RCV001275115]\|WNT10A-related disorder [RCV004535236]\|not provided [RCV000254848]	pathogenic	2	218890349	218890349	Human	4	name , alternate_id
401918874	CV2798078	single nucleotide variant	NM_025216.3(WNT10A):c.112A>T (p.Arg38Trp)	WNT10A-related disorder [RCV004527830]	uncertain significance	2	218881107	218881107	Human		name , trait , alternate_id
11579634	CV284751	single nucleotide variant	NM_025216.3(WNT10A):c.208C>T (p.Arg70Trp)	Odonto-onycho-dermal dysplasia [RCV000401069]\|Odonto-onycho-dermal dysplasia [RCV000639740]\|SchC6pf-Schulz-Passarge syndrome [RCV000308592]\|Tooth agenesis, selective, 4 [RCV000358786]\|WNT10A-related disorder [RCV004530357]\|not provided [RCV001545215]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	218882255	218882255	Human	3	name , alternate_id
11578534	CV284754	single nucleotide variant	NM_025216.3(WNT10A):c.493G>A (p.Gly165Arg)	Odonto-onycho-dermal dysplasia [RCV000346906]\|Odonto-onycho-dermal dysplasia [RCV001083663]\|SchC6pf-Schulz-Passarge syndrome [RCV000283655]\|Tooth agenesis [RCV000845116]\|Tooth agenesis, selective, 4 [RCV000406139]\|WNT10A-related disorder [RCV004530358]\|not provi ... (more) ded [RCV000521785]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	218890100	218890100	Human	5	name , alternate_id
11584307	CV285420	single nucleotide variant	NM_025216.3(WNT10A):c.817C>A (p.Leu273Ile)	Odonto-onycho-dermal dysplasia [RCV000309072]\|Odonto-onycho-dermal dysplasia [RCV000539438]\|SchC6pf-Schulz-Passarge syndrome [RCV000272729]\|Tooth agenesis, selective, 4 [RCV000358737]\|WNT10A-related disorder [RCV004530359]	benign	2	218892834	218892834	Human	3	name , alternate_id
11587627	CV287636	single nucleotide variant	NM_025216.3(WNT10A):c.918C>G (p.Asn306Lys)	Odonto-onycho-dermal dysplasia [RCV000390691]\|Odonto-onycho-dermal dysplasia [RCV000887474]\|SchC6pf-Schulz-Passarge syndrome [RCV000351358]\|Tooth agenesis, selective, 4 [RCV000296501]\|WNT10A-related disorder [RCV004530360]	likely benign	2	218892935	218892935	Human	3	name , alternate_id
405260019	CV3190128	single nucleotide variant	NM_025216.3(WNT10A):c.460C>A (p.Leu154Met)	WNT10A-related disorder [RCV004534653]	uncertain significance	2	218890067	218890067	Human		name , trait , alternate_id
405268842	CV3199059	single nucleotide variant	NM_003394.4(WNT10B):c.798A>G (p.Pro266=)	WNT10B-related disorder [RCV003912164]	likely benign	12	48966467	48966467	Human		name , trait , alternate_id
405292873	CV3207017	indel	NM_025216.3(WNT10A):c.532_537delinsA (p.Gln178fs)	WNT10A-related disorder [RCV004539484]	pathogenic	2	218890139	218890144	Human		trait , alternate_id
405270100	CV3215407	single nucleotide variant	NM_003394.4(WNT10B):c.242A>C (p.His81Pro)	WNT10B-related disorder [RCV003949158]	uncertain significance	12	48970184	48970184	Human		name , trait , alternate_id
405262128	CV3220067	single nucleotide variant	NM_025216.3(WNT10A):c.294C>T (p.His98=)	WNT10A-related disorder [RCV004540779]	likely benign	2	218882341	218882341	Human		name , trait , alternate_id
408385197	CV3505800	single nucleotide variant	NM_003394.4(WNT10B):c.275G>T (p.Trp92Leu)	WNT10B-related disorder [RCV004732435]	uncertain significance	12	48970151	48970151	Human		name , trait , alternate_id
408367473	CV3516176	single nucleotide variant	NM_003394.4(WNT10B):c.661C>T (p.Arg221Trp)	WNT10B-related disorder [RCV004758551]	uncertain significance	12	48967996	48967996	Human		name , trait , alternate_id
408368915	CV3516317	single nucleotide variant	NM_025216.3(WNT10A):c.390C>G (p.Ser130Arg)	WNT10A-related disorder [RCV004736020]	uncertain significance	2	218889997	218889997	Human		name , trait , alternate_id
12742172	CV359415	single nucleotide variant	NM_025216.3(WNT10A):c.337C>T (p.Arg113Cys)	Odonto-onycho-dermal dysplasia [RCV001080960]\|Tooth agenesis, selective, 4 [RCV000991159]\|WNT10A-related disorder [RCV004530509]\|not provided [RCV000413047]	pathogenic\|likely pathogenic\|likely benign\|conflicting interpretations of pathogenicity	2	218882384	218882384	Human	2	name , alternate_id
12907021	CV414868	single nucleotide variant	NM_025216.3(WNT10A):c.661G>A (p.Gly221Arg)	Odonto-onycho-dermal dysplasia [RCV001037834]\|WNT10A-related disorder [RCV004541539]\|not provided [RCV000489933]\|not specified [RCV003323568]	pathogenic\|likely pathogenic\|uncertain significance	2	218890268	218890268	Human	2	name , alternate_id
13534321	CV513099	single nucleotide variant	NM_003394.4(WNT10B):c.676C>T (p.Arg226Ter)	Split hand-foot malformation 6 [RCV000625580]\|WNT10B-related disorder [RCV004758043]	pathogenic\|likely pathogenic	12	48967981	48967981	Human	1	name , alternate_id
13816786	CV559113	single nucleotide variant	NM_025216.3(WNT10A):c.205C>T (p.Arg69Trp)	Odonto-onycho-dermal dysplasia [RCV000706597]\|SchC6pf-Schulz-Passarge syndrome [RCV001825402]\|WNT10A-related disorder [RCV004544952]	uncertain significance	2	218882252	218882252	Human	3	name , alternate_id
15143319	CV691031	single nucleotide variant	NM_025216.3(WNT10A):c.512G>A (p.Arg171His)	Odonto-onycho-dermal dysplasia [RCV000878034]\|SchC6pf-Schulz-Passarge syndrome [RCV001825777]\|WNT10A-related disorder [RCV004530879]	likely benign	2	218890119	218890119	Human	3	name , alternate_id
15130389	CV713550	single nucleotide variant	NM_003394.4(WNT10B):c.901C>T (p.Pro301Ser)	WNT10B-related disorder [RCV003916155]\|not provided [RCV000964427]\|not specified [RCV001724198]	benign	12	48966364	48966364	Human	1	name , alternate_id
15113264	CV781184	single nucleotide variant	NM_025216.3(WNT10A):c.891C>G (p.Ala297=)	Odonto-onycho-dermal dysplasia [RCV000977988]\|SchC6pf-Schulz-Passarge syndrome [RCV001836048]\|WNT10A-related disorder [RCV004543647]	likely benign	2	218892908	218892908	Human	3	name , alternate_id
8624623	CV79734	single nucleotide variant	NM_025216.3(WNT10A):c.283G>A (p.Glu95Lys)	Odonto-onycho-dermal dysplasia [RCV000811807]\|SchC6pf-Schulz-Passarge syndrome [RCV001275113]\|Tooth agenesis, selective, 4 [RCV002292375]\|WNT10A-related disorder [RCV004542736]\|not provided [RCV000059802]	pathogenic\|likely pathogenic\|uncertain significance\|not provided	2	218882330	218882330	Human	3	name , alternate_id
28896847	CV883764	single nucleotide variant	NM_025216.3(WNT10A):c.364A>T (p.Ile122Phe)	Odonto-onycho-dermal dysplasia [RCV001141382]\|Odonto-onycho-dermal dysplasia [RCV002559369]\|SchC6pf-Schulz-Passarge syndrome [RCV001141381]\|Tooth agenesis, selective, 4 [RCV001141383]\|WNT10A-related disorder [RCV004734028]	uncertain significance	2	218882411	218882411	Human	3	name , alternate_id
28901566	CV883765	single nucleotide variant	NM_025216.3(WNT10A):c.443C>T (p.Ala148Val)	Odonto-onycho-dermal dysplasia [RCV001143234]\|Odonto-onycho-dermal dysplasia [RCV002559384]\|SchC6pf-Schulz-Passarge syndrome [RCV001143233]\|Tooth agenesis, selective, 4 [RCV001143235]\|WNT10A-related disorder [RCV004734030]	uncertain significance	2	218890050	218890050	Human	3	name , alternate_id
28897527	CV883773	single nucleotide variant	NM_025216.3(WNT10A):c.719C>T (p.Ala240Val)	Odonto-onycho-dermal dysplasia [RCV001141618]\|Odonto-onycho-dermal dysplasia [RCV001487964]\|Odonto-onycho-dermal dysplasia [RCV005021481]\|SchC6pf-Schulz-Passarge syndrome [RCV001141620]\|Tooth agenesis, selective, 4 [RCV001141619]\|WNT10A-related disorder [RCV0047 ... (more) 34029]	likely benign\|uncertain significance	2	218890326	218890326	Human	3	name , alternate_id
156207005	CV1990616	single nucleotide variant	NM_025216.3(WNT10A):c.21C>T (p.Arg7=)	Odonto-onycho-dermal dysplasia [RCV002625938]	likely benign	2	218881016	218881016	Human	1	name
404992786	CV3091445	single nucleotide variant	NM_025216.3(WNT10A):c.21C>G (p.Arg7=)	Odonto-onycho-dermal dysplasia [RCV003792920]	likely benign	2	218881016	218881016	Human	1	name
407524799	CV3487971	single nucleotide variant	NM_057168.2(WNT16):c.5A>G (p.Asp2Gly)	not specified [RCV004678562]	uncertain significance	7	121329297	121329297	Human		name
127267960	CV1069098	single nucleotide variant	NM_025216.3(WNT10A):c.45G>A (p.Gln15=)	Odonto-onycho-dermal dysplasia [RCV001404284]	likely benign	2	218881040	218881040	Human	1	name
127301039	CV1112302	single nucleotide variant	NM_025216.3(WNT10A):c.36C>T (p.Leu12=)	Odonto-onycho-dermal dysplasia [RCV001454038]	likely benign	2	218881031	218881031	Human	1	name
151842402	CV1359301	single nucleotide variant	NM_025216.3(WNT10A):c.7A>T (p.Ser3Cys)	Odonto-onycho-dermal dysplasia [RCV002015495]	uncertain significance	2	218881002	218881002	Human	1	name
151708828	CV1448881	single nucleotide variant	NM_025216.3(WNT10A):c.1A>T (p.Met1Leu)	Odonto-onycho-dermal dysplasia [RCV001963872]\|Odonto-onycho-dermal dysplasia [RCV005025545]	pathogenic\|likely pathogenic	2	218880996	218880996	Human	1	name
152148852	CV1528963	single nucleotide variant	NM_025216.3(WNT10A):c.42C>A (p.Pro14=)	Odonto-onycho-dermal dysplasia [RCV002101905]	likely benign	2	218881037	218881037	Human	1	name
152169819	CV1546602	single nucleotide variant	NM_025216.3(WNT10A):c.94C>T (p.Leu32=)	Odonto-onycho-dermal dysplasia [RCV002142913]	likely benign	2	218881089	218881089	Human	1	name
152099286	CV1606515	single nucleotide variant	NM_025216.3(WNT10A):c.54G>A (p.Pro18=)	Odonto-onycho-dermal dysplasia [RCV002195330]	likely benign	2	218881049	218881049	Human	1	name
152051596	CV1607103	single nucleotide variant	NM_025216.3(WNT10A):c.88C>T (p.Leu30=)	Odonto-onycho-dermal dysplasia [RCV002109038]	likely benign	2	218881083	218881083	Human	1	name
152062520	CV1638669	single nucleotide variant	NM_025216.3(WNT10A):c.72G>A (p.Val24=)	Odonto-onycho-dermal dysplasia [RCV002073848]	likely benign	2	218881067	218881067	Human	1	name
156300948	CV1916091	single nucleotide variant	NM_025216.3(WNT10A):c.36C>G (p.Leu12=)	Odonto-onycho-dermal dysplasia [RCV002599168]	likely benign	2	218881031	218881031	Human	1	name
156340377	CV1961648	single nucleotide variant	NM_025216.3(WNT10A):c.3G>A (p.Met1Ile)	Odonto-onycho-dermal dysplasia [RCV002580474]	likely pathogenic	2	218880998	218880998	Human	1	name
156117087	CV1982561	single nucleotide variant	NM_025216.3(WNT10A):c.90G>C (p.Leu30=)	Odonto-onycho-dermal dysplasia [RCV002622801]	likely benign	2	218881085	218881085	Human	1	name
156004665	CV2014954	single nucleotide variant	NM_025216.3(WNT10A):c.72G>T (p.Val24=)	Odonto-onycho-dermal dysplasia [RCV002690214]	likely benign	2	218881067	218881067	Human	1	name
156375274	CV2024635	single nucleotide variant	NM_025216.3(WNT10A):c.39A>T (p.Arg13=)	Odonto-onycho-dermal dysplasia [RCV002721866]	likely benign	2	218881034	218881034	Human	1	name
155938740	CV2146478	single nucleotide variant	NM_025216.3(WNT10A):c.75C>G (p.Leu25=)	Odonto-onycho-dermal dysplasia [RCV003014123]	likely benign	2	218881070	218881070	Human	1	name
155969359	CV2152432	single nucleotide variant	NM_025216.3(WNT10A):c.54G>C (p.Pro18=)	Odonto-onycho-dermal dysplasia [RCV003015858]	likely benign	2	218881049	218881049	Human	1	name
11587088	CV287875	single nucleotide variant	NM_025216.3(WNT10A):c.85C>T (p.Leu29=)	Odonto-onycho-dermal dysplasia [RCV000352267]\|Odonto-onycho-dermal dysplasia [RCV000554191]\|SchC6pf-Schulz-Passarge syndrome [RCV000397831]\|Tooth agenesis, selective, 4 [RCV000292419]	benign\|likely benign	2	218881080	218881080	Human	3	name
405004327	CV3082662	single nucleotide variant	NM_025216.3(WNT10A):c.87A>G (p.Leu29=)	Odonto-onycho-dermal dysplasia [RCV003783761]	likely benign	2	218881082	218881082	Human	1	name
405007662	CV3083103	single nucleotide variant	NM_025216.3(WNT10A):c.78G>C (p.Leu26=)	Odonto-onycho-dermal dysplasia [RCV003784050]	likely benign	2	218881073	218881073	Human	1	name
402525364	CV3086738	single nucleotide variant	NM_025216.3(WNT10A):c.76C>T (p.Leu26=)	Odonto-onycho-dermal dysplasia [RCV003781355]	likely benign	2	218881071	218881071	Human	1	name
404983819	CV3087175	single nucleotide variant	NM_025216.3(WNT10A):c.75C>T (p.Leu25=)	Odonto-onycho-dermal dysplasia [RCV003781638]	likely benign	2	218881070	218881070	Human	1	name
402508702	CV3088833	single nucleotide variant	NM_025216.3(WNT10A):c.1A>G (p.Met1Val)	Odonto-onycho-dermal dysplasia [RCV003780037]	pathogenic	2	218880996	218880996	Human	1	name
402485759	CV3093824	single nucleotide variant	NM_025216.3(WNT10A):c.81C>T (p.Phe27=)	Odonto-onycho-dermal dysplasia [RCV003787025]	likely benign	2	218881076	218881076	Human	1	name
405075964	CV3100289	single nucleotide variant	NM_025216.3(WNT10A):c.63G>T (p.Ala21=)	Odonto-onycho-dermal dysplasia [RCV003799842]	likely benign	2	218881058	218881058	Human	1	name
405176305	CV3101149	single nucleotide variant	NM_025216.3(WNT10A):c.33G>A (p.Arg11=)	Odonto-onycho-dermal dysplasia [RCV003803536]	likely benign	2	218881028	218881028	Human	1	name
405082982	CV3107519	single nucleotide variant	NM_025216.3(WNT10A):c.78G>A (p.Leu26=)	Odonto-onycho-dermal dysplasia [RCV003800389]	likely benign	2	218881073	218881073	Human	1	name
405157116	CV3109396	single nucleotide variant	NM_025216.3(WNT10A):c.78G>T (p.Leu26=)	Odonto-onycho-dermal dysplasia [RCV003801920]	likely benign	2	218881073	218881073	Human	1	name
405005339	CV3120825	single nucleotide variant	NM_003394.4(WNT10B):c.87T>C (p.Asn29=)	not provided [RCV003828428]	likely benign	12	48970339	48970339	Human		name
407524802	CV3487972	single nucleotide variant	NM_057168.2(WNT16):c.10G>C (p.Ala4Pro)	not specified [RCV004678563]	uncertain significance	7	121329302	121329302	Human		name
15147097	CV691029	single nucleotide variant	NM_025216.3(WNT10A):c.4G>A (p.Gly2Ser)	Odonto-onycho-dermal dysplasia [RCV000878679]\|SchC6pf-Schulz-Passarge syndrome [RCV001277356]\|not provided [RCV004711361]	benign\|likely benign	2	218880999	218880999	Human	3	name
15180172	CV738294	single nucleotide variant	NM_004626.3(WNT11):c.216C>T (p.Ala72=)	not provided [RCV000907287]	benign	11	76196586	76196586	Human		name
15162703	CV738666	single nucleotide variant	NM_003394.4(WNT10B):c.36G>A (p.Ser12=)	not provided [RCV000903611]	benign	12	48970494	48970494	Human		name
8634379	CV89599	single nucleotide variant	NM_004626.2(WNT11):c.246G>A (p.Arg82=)	Malignant melanoma [RCV000069696]	not provided	11	76196556	76196556	Human		name
127243551	CV1069099	single nucleotide variant	NM_025216.3(WNT10A):c.159C>T (p.Pro53=)	Odonto-onycho-dermal dysplasia [RCV001398399]	likely benign	2	218882206	218882206	Human	1	name
127272333	CV1069100	single nucleotide variant	NM_025216.3(WNT10A):c.201G>A (p.Leu67=)	Odonto-onycho-dermal dysplasia [RCV001405688]	likely benign	2	218882248	218882248	Human	1	name
127250451	CV1090783	single nucleotide variant	NM_025216.3(WNT10A):c.282C>T (p.His94=)	Odonto-onycho-dermal dysplasia [RCV001436341]	likely benign	2	218882329	218882329	Human	1	name
127300594	CV1112303	single nucleotide variant	NM_025216.3(WNT10A):c.135G>T (p.Leu45=)	Odonto-onycho-dermal dysplasia [RCV001461132]	likely benign	2	218882182	218882182	Human	1	name
127304461	CV1112304	single nucleotide variant	NM_025216.3(WNT10A):c.150C>A (p.Pro50=)	Odonto-onycho-dermal dysplasia [RCV001454971]	likely benign	2	218882197	218882197	Human	1	name
127303357	CV1112305	single nucleotide variant	NM_025216.3(WNT10A):c.150C>T (p.Pro50=)	Odonto-onycho-dermal dysplasia [RCV001461911]	likely benign	2	218882197	218882197	Human	1	name
127293494	CV1112306	single nucleotide variant	NM_025216.3(WNT10A):c.168T>C (p.Asn56=)	Odonto-onycho-dermal dysplasia [RCV001476605]	likely benign	2	218882215	218882215	Human	1	name
127309196	CV1133219	single nucleotide variant	NM_025216.3(WNT10A):c.190T>C (p.Leu64=)	Odonto-onycho-dermal dysplasia [RCV001500983]	likely benign	2	218882237	218882237	Human	1	name
127298716	CV1133220	single nucleotide variant	NM_025216.3(WNT10A):c.199C>T (p.Leu67=)	Odonto-onycho-dermal dysplasia [RCV001498137]	likely benign	2	218882246	218882246	Human	1	name
127286980	CV1133221	single nucleotide variant	NM_025216.3(WNT10A):c.201G>C (p.Leu67=)	Odonto-onycho-dermal dysplasia [RCV001494653]	likely benign	2	218882248	218882248	Human	1	name
127287187	CV1133222	single nucleotide variant	NM_025216.3(WNT10A):c.273C>A (p.Ile91=)	Odonto-onycho-dermal dysplasia [RCV001494793]	likely benign	2	218882320	218882320	Human	1	name
127297202	CV1133223	single nucleotide variant	NM_025216.3(WNT10A):c.279C>T (p.Ile93=)	Odonto-onycho-dermal dysplasia [RCV001497722]	likely benign	2	218882326	218882326	Human	1	name
151828862	CV1480044	deletion	NM_025216.3(WNT10A):c.85del (p.Leu29fs)	Odonto-onycho-dermal dysplasia [RCV001901602]	pathogenic	2	218881079	218881079	Human	1	name
152044888	CV1535584	single nucleotide variant	NM_025216.3(WNT10A):c.276C>T (p.Ala92=)	Odonto-onycho-dermal dysplasia [RCV002166163]	likely benign	2	218882323	218882323	Human	1	name
152050709	CV1606965	single nucleotide variant	NM_025216.3(WNT10A):c.186A>G (p.Leu62=)	Odonto-onycho-dermal dysplasia [RCV002108932]	likely benign	2	218882233	218882233	Human	1	name
152105980	CV1612699	single nucleotide variant	NM_025216.3(WNT10A):c.138C>T (p.Asp46=)	Odonto-onycho-dermal dysplasia [RCV002173721]	likely benign	2	218882185	218882185	Human	1	name
152157438	CV1615925	single nucleotide variant	NM_025216.3(WNT10A):c.288C>T (p.Cys96=)	Odonto-onycho-dermal dysplasia [RCV002159030]	likely benign	2	218882335	218882335	Human	1	name
152084774	CV1617121	single nucleotide variant	NM_025216.3(WNT10A):c.297A>G (p.Gln99=)	Odonto-onycho-dermal dysplasia [RCV002076839]	likely benign	2	218882344	218882344	Human	1	name
152085308	CV1633453	single nucleotide variant	NM_025216.3(WNT10A):c.177A>T (p.Thr59=)	Odonto-onycho-dermal dysplasia [RCV002113303]	likely benign	2	218882224	218882224	Human	1	name
152101316	CV1649009	single nucleotide variant	NM_025216.3(WNT10A):c.184C>T (p.Leu62=)	Odonto-onycho-dermal dysplasia [RCV002214047]	likely benign	2	218882231	218882231	Human	1	name
152079952	CV1666875	single nucleotide variant	NM_003394.4(WNT10B):c.288G>A (p.Ala96=)	not provided [RCV002211220]	benign\|likely benign	12	48970138	48970138	Human		name
8558103	CV19504	single nucleotide variant	NM_025216.3(WNT10A):c.27G>A (p.Trp9Ter)	Odonto-onycho-dermal dysplasia [RCV000004720]	pathogenic	2	218881022	218881022	Human	1	name
155978206	CV2081673	single nucleotide variant	NM_025216.3(WNT10A):c.133C>T (p.Leu45=)	Odonto-onycho-dermal dysplasia [RCV002863636]	likely benign	2	218882180	218882180	Human	1	name
156023566	CV2141485	single nucleotide variant	NM_025216.3(WNT10A):c.132T>A (p.Ile44=)	Odonto-onycho-dermal dysplasia [RCV002976272]	likely benign	2	218882179	218882179	Human	1	name
156000003	CV2378653	single nucleotide variant	NM_004626.3(WNT11):c.78G>C (p.Lys26Asn)	not specified [RCV004231124]	uncertain significance	11	76206330	76206330	Human		name
329401794	CV2457426	single nucleotide variant	NM_004626.3(WNT11):c.76A>G (p.Lys26Glu)	not specified [RCV004267251]	uncertain significance	11	76206332	76206332	Human		name
401796952	CV2741878	single nucleotide variant	NM_025216.3(WNT10A):c.26G>A (p.Trp9Ter)	Tooth agenesis, selective, 4 [RCV003323310]	pathogenic	2	218881021	218881021	Human	1	name
405228185	CV3036483	single nucleotide variant	NM_003394.4(WNT10B):c.255C>T (p.His85=)	not provided [RCV003710974]	likely benign	12	48970171	48970171	Human		name
405022461	CV3088186	single nucleotide variant	NM_025216.3(WNT10A):c.208C>A (p.Arg70=)	Odonto-onycho-dermal dysplasia [RCV003795746]	likely benign	2	218882255	218882255	Human	1	name
404988608	CV3097101	single nucleotide variant	NM_025216.3(WNT10A):c.174C>T (p.Asn58=)	Odonto-onycho-dermal dysplasia [RCV003792490]	likely benign	2	218882221	218882221	Human	1	name
405028213	CV3098151	single nucleotide variant	NM_025216.3(WNT10A):c.162G>A (p.Val54=)	Odonto-onycho-dermal dysplasia [RCV003806444]	likely benign	2	218882209	218882209	Human	1	name
405085144	CV3104514	single nucleotide variant	NM_025216.3(WNT10A):c.111C>T (p.Pro37=)	Odonto-onycho-dermal dysplasia [RCV003800572]	likely benign	2	218881106	218881106	Human	1	name
405160501	CV3109796	single nucleotide variant	NM_025216.3(WNT10A):c.243G>A (p.Val81=)	Odonto-onycho-dermal dysplasia [RCV003802155]	likely benign	2	218882290	218882290	Human	1	name
405110840	CV3110685	single nucleotide variant	NM_025216.3(WNT10A):c.105C>G (p.Ala35=)	Odonto-onycho-dermal dysplasia [RCV003813588]	likely benign	2	218881100	218881100	Human	1	name
405108488	CV3112323	single nucleotide variant	NM_025216.3(WNT10A):c.219G>A (p.Glu73=)	Odonto-onycho-dermal dysplasia [RCV003813166]	likely benign	2	218882266	218882266	Human	1	name
407524779	CV3487959	single nucleotide variant	NM_025216.3(WNT10A):c.19C>A (p.Arg7Ser)	Inborn genetic diseases [RCV004678553]	uncertain significance	2	218881014	218881014	Human	1	name
597799995	CV3624211	single nucleotide variant	NM_057168.2(WNT16):c.31C>G (p.Arg11Gly)	not specified [RCV004879972]	uncertain significance	7	121329323	121329323	Human		name
597857244	CV3877772	single nucleotide variant	NM_025216.3(WNT10A):c.156G>A (p.Glu52=)	Odonto-onycho-dermal dysplasia [RCV005229081]	likely benign	2	218882203	218882203	Human	1	name
15126153	CV691030	single nucleotide variant	NM_025216.3(WNT10A):c.234C>T (p.His78=)	Odonto-onycho-dermal dysplasia [RCV000875071]\|Odonto-onycho-dermal dysplasia [RCV001138801]\|SchC6pf-Schulz-Passarge syndrome [RCV001138803]\|Tooth agenesis, selective, 4 [RCV001138802]	benign\|likely benign	2	218882281	218882281	Human	3	name
15121546	CV710732	single nucleotide variant	NM_057168.2(WNT16):c.300C>A (p.Thr100=)	not provided [RCV000962913]	benign	7	121329771	121329771	Human		name
15180236	CV713184	single nucleotide variant	NM_004626.3(WNT11):c.813G>T (p.Ser271=)	not provided [RCV000974102]	benign	11	76191641	76191641	Human		name
15134958	CV713185	single nucleotide variant	NM_004626.3(WNT11):c.813G>A (p.Ser271=)	not provided [RCV000965209]	benign	11	76191641	76191641	Human		name
15188115	CV738293	single nucleotide variant	NM_004626.3(WNT11):c.633C>T (p.Cys211=)	not provided [RCV000909277]	benign	11	76191821	76191821	Human		name
15136552	CV747301	single nucleotide variant	NM_025216.3(WNT10A):c.273C>T (p.Ile91=)	Odonto-onycho-dermal dysplasia [RCV000921029]	likely benign	2	218882320	218882320	Human	1	name
15119144	CV781181	single nucleotide variant	NM_025216.3(WNT10A):c.267C>A (p.Ile89=)	Odonto-onycho-dermal dysplasia [RCV000979069]	likely benign	2	218882314	218882314	Human	1	name
127260638	CV1059188	duplication	NM_025216.3(WNT10A):c.143dup (p.Leu49fs)	Odonto-onycho-dermal dysplasia [RCV001387393]	pathogenic	2	218882189	218882190	Human		name
127236287	CV1059189	deletion	NM_025216.3(WNT10A):c.295del (p.Gln99fs)	Odonto-onycho-dermal dysplasia [RCV001382583]	pathogenic	2	218882341	218882341	Human	1	name
127234275	CV1069101	single nucleotide variant	NM_025216.3(WNT10A):c.420C>A (p.Gly140=)	Odonto-onycho-dermal dysplasia [RCV001414178]	likely benign	2	218890027	218890027	Human	1	name
127264579	CV1069102	single nucleotide variant	NM_025216.3(WNT10A):c.544C>T (p.Leu182=)	Odonto-onycho-dermal dysplasia [RCV001403334]	likely benign	2	218890151	218890151	Human	1	name
127242066	CV1069104	single nucleotide variant	NM_025216.3(WNT10A):c.717C>T (p.His239=)	Odonto-onycho-dermal dysplasia [RCV001393279]	likely benign	2	218890324	218890324	Human	1	name
127260375	CV1069105	single nucleotide variant	NM_025216.3(WNT10A):c.816G>A (p.Gln272=)	Odonto-onycho-dermal dysplasia [RCV001420037]	likely benign	2	218892833	218892833	Human	1	name
127230702	CV1069106	single nucleotide variant	NM_025216.3(WNT10A):c.906G>A (p.Pro302=)	Odonto-onycho-dermal dysplasia [RCV001412633]	likely benign	2	218892923	218892923	Human	1	name
127270681	CV1069107	single nucleotide variant	NM_025216.3(WNT10A):c.966G>C (p.Pro322=)	Odonto-onycho-dermal dysplasia [RCV001405080]\|SchC6pf-Schulz-Passarge syndrome [RCV001826205]	likely benign	2	218892983	218892983	Human	3	name
127272110	CV1090784	single nucleotide variant	NM_025216.3(WNT10A):c.372C>T (p.Ser124=)	Odonto-onycho-dermal dysplasia [RCV001431190]	likely benign	2	218882419	218882419	Human	1	name
127284277	CV1090785	single nucleotide variant	NM_025216.3(WNT10A):c.402C>T (p.Tyr134=)	Odonto-onycho-dermal dysplasia [RCV001449215]\|Odonto-onycho-dermal dysplasia [RCV002495635]	likely benign	2	218890009	218890009	Human	1	name
127260617	CV1090787	single nucleotide variant	NM_025216.3(WNT10A):c.432C>T (p.Ala144=)	Odonto-onycho-dermal dysplasia [RCV001438636]	likely benign	2	218890039	218890039	Human	1	name
127273733	CV1090788	single nucleotide variant	NM_025216.3(WNT10A):c.465G>A (p.Lys155=)	Odonto-onycho-dermal dysplasia [RCV001431709]	likely benign	2	218890072	218890072	Human	1	name
127255959	CV1090789	single nucleotide variant	NM_025216.3(WNT10A):c.477T>C (p.Cys159=)	Odonto-onycho-dermal dysplasia [RCV001426717]	likely benign	2	218890084	218890084	Human	1	name
127243767	CV1090790	single nucleotide variant	NM_025216.3(WNT10A):c.525C>T (p.His175=)	Odonto-onycho-dermal dysplasia [RCV001424012]	likely benign	2	218890132	218890132	Human	1	name
127247119	CV1090791	single nucleotide variant	NM_025216.3(WNT10A):c.555T>C (p.Gly185=)	Odonto-onycho-dermal dysplasia [RCV001424621]	likely benign	2	218890162	218890162	Human	1	name
127236734	CV1090792	single nucleotide variant	NM_025216.3(WNT10A):c.567C>T (p.Ser189=)	Odonto-onycho-dermal dysplasia [RCV001433403]	likely benign	2	218890174	218890174	Human	1	name
127263812	CV1090793	single nucleotide variant	NM_025216.3(WNT10A):c.609A>G (p.Pro203=)	Odonto-onycho-dermal dysplasia [RCV001439413]	likely benign	2	218890216	218890216	Human	1	name
127265692	CV1090795	single nucleotide variant	NM_025216.3(WNT10A):c.775C>A (p.Arg259=)	Odonto-onycho-dermal dysplasia [RCV001429167]\|SchC6pf-Schulz-Passarge syndrome [RCV001831485]	likely benign	2	218892792	218892792	Human	3	name
127265814	CV1090796	single nucleotide variant	NM_025216.3(WNT10A):c.813C>T (p.Cys271=)	Odonto-onycho-dermal dysplasia [RCV001440081]	likely benign	2	218892830	218892830	Human	1	name
127242525	CV1090797	single nucleotide variant	NM_025216.3(WNT10A):c.855C>T (p.Thr285=)	Odonto-onycho-dermal dysplasia [RCV001434661]	likely benign	2	218892872	218892872	Human	1	name
127298959	CV1112307	single nucleotide variant	NM_025216.3(WNT10A):c.327C>T (p.Ser109=)	Odonto-onycho-dermal dysplasia [RCV001478025]	likely benign	2	218882374	218882374	Human	1	name
127329394	CV1112308	single nucleotide variant	NM_025216.3(WNT10A):c.348C>T (p.Ile116=)	Odonto-onycho-dermal dysplasia [RCV001470184]	likely benign	2	218882395	218882395	Human	1	name
127318154	CV1112309	single nucleotide variant	NM_025216.3(WNT10A):c.438C>T (p.Ser146=)	Odonto-onycho-dermal dysplasia [RCV001466091]	likely benign	2	218890045	218890045	Human	1	name
127322360	CV1112310	single nucleotide variant	NM_025216.3(WNT10A):c.561C>T (p.Gly187=)	Odonto-onycho-dermal dysplasia [RCV001467558]	likely benign	2	218890168	218890168	Human	1	name
127305122	CV1112311	single nucleotide variant	NM_025216.3(WNT10A):c.576C>T (p.Val192=)	Odonto-onycho-dermal dysplasia [RCV001455168]	likely benign	2	218890183	218890183	Human	1	name
127323149	CV1112312	single nucleotide variant	NM_025216.3(WNT10A):c.594G>A (p.Leu198=)	Odonto-onycho-dermal dysplasia [RCV001467817]	likely benign	2	218890201	218890201	Human	1	name
127300474	CV1112313	single nucleotide variant	NM_025216.3(WNT10A):c.690C>T (p.Asp230=)	Odonto-onycho-dermal dysplasia [RCV001453905]	likely benign	2	218890297	218890297	Human	1	name
127300261	CV1112314	single nucleotide variant	NM_025216.3(WNT10A):c.738C>T (p.Asn246=)	Odonto-onycho-dermal dysplasia [RCV001453822]	likely benign	2	218890345	218890345	Human	1	name
127296858	CV1112315	single nucleotide variant	NM_025216.3(WNT10A):c.936G>A (p.Pro312=)	Odonto-onycho-dermal dysplasia [RCV001452872]	likely benign	2	218892953	218892953	Human	1	name
127312830	CV1133217	single nucleotide variant	NM_025216.3(WNT10A):c.62C>G (p.Ala21Gly)	Inborn genetic diseases [RCV004686675]\|Odonto-onycho-dermal dysplasia [RCV001481787]	likely benign\|uncertain significance	2	218881057	218881057	Human	2	name
127334360	CV1133224	single nucleotide variant	NM_025216.3(WNT10A):c.363C>T (p.Pro121=)	Odonto-onycho-dermal dysplasia [RCV001490778]	likely benign	2	218882410	218882410	Human	1	name
127310307	CV1133225	single nucleotide variant	NM_025216.3(WNT10A):c.423G>C (p.Val141=)	Odonto-onycho-dermal dysplasia [RCV001481110]	likely benign	2	218890030	218890030	Human	1	name
127337308	CV1133227	single nucleotide variant	NM_025216.3(WNT10A):c.606C>T (p.Ser202=)	Odonto-onycho-dermal dysplasia [RCV001492777]	likely benign	2	218890213	218890213	Human	1	name
127322983	CV1133228	single nucleotide variant	NM_025216.3(WNT10A):c.648C>T (p.Pro216=)	Odonto-onycho-dermal dysplasia [RCV001485117]	likely benign	2	218890255	218890255	Human	1	name
127334815	CV1133229	single nucleotide variant	NM_025216.3(WNT10A):c.720G>A (p.Ala240=)	Odonto-onycho-dermal dysplasia [RCV001491124]	likely benign	2	218890327	218890327	Human	1	name
127317018	CV1133232	single nucleotide variant	NM_025216.3(WNT10A):c.939C>T (p.Gly313=)	Odonto-onycho-dermal dysplasia [RCV001483042]	likely benign	2	218892956	218892956	Human	1	name
127319019	CV1133233	single nucleotide variant	NM_025216.3(WNT10A):c.999C>G (p.Pro333=)	Odonto-onycho-dermal dysplasia [RCV001503897]	likely benign	2	218893016	218893016	Human	1	name
151753513	CV1508683	single nucleotide variant	NM_025216.3(WNT10A):c.456C>T (p.Gly152=)	Odonto-onycho-dermal dysplasia [RCV001986530]\|Odonto-onycho-dermal dysplasia [RCV004555896]	likely benign\|uncertain significance	2	218890063	218890063	Human	1	name
152082812	CV1526254	single nucleotide variant	NM_025216.3(WNT10A):c.843C>T (p.Pro281=)	Odonto-onycho-dermal dysplasia [RCV002170763]	likely benign	2	218892860	218892860	Human	1	name
152109955	CV1530155	single nucleotide variant	NM_025216.3(WNT10A):c.681C>T (p.Asp227=)	Odonto-onycho-dermal dysplasia [RCV002196636]	likely benign	2	218890288	218890288	Human	1	name
152076567	CV1531176	single nucleotide variant	NM_025216.3(WNT10A):c.558G>A (p.Lys186=)	Odonto-onycho-dermal dysplasia [RCV002210675]	likely benign	2	218890165	218890165	Human	1	name
152122061	CV1547692	single nucleotide variant	NM_025216.3(WNT10A):c.855C>A (p.Thr285=)	Odonto-onycho-dermal dysplasia [RCV002081689]	likely benign	2	218892872	218892872	Human	1	name
152126109	CV1548823	single nucleotide variant	NM_025216.3(WNT10A):c.613C>T (p.Leu205=)	Odonto-onycho-dermal dysplasia [RCV002082237]	likely benign	2	218890220	218890220	Human	1	name
152170899	CV1552449	single nucleotide variant	NM_025216.3(WNT10A):c.351C>T (p.Pro117=)	Odonto-onycho-dermal dysplasia [RCV002143271]	likely benign	2	218882398	218882398	Human	1	name
152116025	CV1553335	single nucleotide variant	NM_025216.3(WNT10A):c.468C>T (p.Ala156=)	Odonto-onycho-dermal dysplasia [RCV002080904]	likely benign	2	218890075	218890075	Human	1	name
152140497	CV1555853	single nucleotide variant	NM_025216.3(WNT10A):c.645C>T (p.Ser215=)	Odonto-onycho-dermal dysplasia [RCV002200510]	likely benign	2	218890252	218890252	Human	1	name
152173831	CV1568585	single nucleotide variant	NM_003394.4(WNT10B):c.396A>T (p.Val132=)	not provided [RCV002184308]	likely benign	12	48968261	48968261	Human		name
152078741	CV1579742	single nucleotide variant	NM_025216.3(WNT10A):c.450C>A (p.Ala150=)	Odonto-onycho-dermal dysplasia [RCV002076085]	likely benign	2	218890057	218890057	Human	1	name
152110843	CV1581765	single nucleotide variant	NM_025216.3(WNT10A):c.942A>G (p.Pro314=)	Odonto-onycho-dermal dysplasia [RCV002096827]	likely benign	2	218892959	218892959	Human	1	name
152055309	CV1582083	single nucleotide variant	NM_025216.3(WNT10A):c.474C>T (p.Gly158=)	Odonto-onycho-dermal dysplasia [RCV002089634]	likely benign	2	218890081	218890081	Human	1	name
152157609	CV1586236	single nucleotide variant	NM_025216.3(WNT10A):c.777G>T (p.Arg259=)	Odonto-onycho-dermal dysplasia [RCV002140367]	likely benign	2	218892794	218892794	Human	1	name
152118804	CV1593545	single nucleotide variant	NM_025216.3(WNT10A):c.483G>A (p.Ala161=)	Odonto-onycho-dermal dysplasia [RCV002097865]	likely benign	2	218890090	218890090	Human	1	name
152090540	CV1594103	single nucleotide variant	NM_025216.3(WNT10A):c.951A>G (p.Ala317=)	Odonto-onycho-dermal dysplasia [RCV002171764]	likely benign	2	218892968	218892968	Human	1	name
152088131	CV1594803	single nucleotide variant	NM_025216.3(WNT10A):c.540T>C (p.Asp180=)	Odonto-onycho-dermal dysplasia [RCV002113694]	likely benign	2	218890147	218890147	Human	1	name
152074897	CV1599322	single nucleotide variant	NM_025216.3(WNT10A):c.489G>A (p.Arg163=)	Odonto-onycho-dermal dysplasia [RCV002075596]	likely benign	2	218890096	218890096	Human	1	name
152083076	CV1623702	single nucleotide variant	NM_025216.3(WNT10A):c.444G>C (p.Ala148=)	Odonto-onycho-dermal dysplasia [RCV002149566]	likely benign	2	218890051	218890051	Human	1	name
152151897	CV1626662	single nucleotide variant	NM_025216.3(WNT10A):c.408C>T (p.Ile136=)	Odonto-onycho-dermal dysplasia [RCV002202098]	likely benign	2	218890015	218890015	Human	1	name
152098145	CV1627015	single nucleotide variant	NM_003394.4(WNT10B):c.47G>A (p.Gly16Asp)	not provided [RCV002095140]	likely benign	12	48970483	48970483	Human		name
152135153	CV1638513	single nucleotide variant	NM_025216.3(WNT10A):c.891C>A (p.Ala297=)	Odonto-onycho-dermal dysplasia [RCV002083404]	likely benign	2	218892908	218892908	Human	1	name
152102959	CV1656820	single nucleotide variant	NM_025216.3(WNT10A):c.930G>A (p.Leu310=)	Odonto-onycho-dermal dysplasia [RCV002195784]	likely benign	2	218892947	218892947	Human	1	name
156010431	CV1880365	single nucleotide variant	NM_025216.3(WNT10A):c.529T>C (p.Leu177=)	Odonto-onycho-dermal dysplasia [RCV003077056]	likely benign	2	218890136	218890136	Human	1	name
156074622	CV1904107	single nucleotide variant	NM_003394.4(WNT10B):c.543C>T (p.Gly181=)	not provided [RCV002591378]	benign	12	48968114	48968114	Human		name
156409215	CV1922547	single nucleotide variant	NM_025216.3(WNT10A):c.819C>T (p.Leu273=)	Odonto-onycho-dermal dysplasia [RCV002607487]	likely benign	2	218892836	218892836	Human	1	name
156360519	CV1925492	single nucleotide variant	NM_025216.3(WNT10A):c.945G>A (p.Ala315=)	Odonto-onycho-dermal dysplasia [RCV002651607]	likely benign	2	218892962	218892962	Human	1	name
156409900	CV1962007	single nucleotide variant	NM_003394.4(WNT10B):c.801G>A (p.Glu267=)	not provided [RCV002586975]	likely benign	12	48966464	48966464	Human		name
156198869	CV1968037	single nucleotide variant	NM_025216.3(WNT10A):c.38G>C (p.Arg13Pro)	Inborn genetic diseases [RCV004065691]\|Odonto-onycho-dermal dysplasia [RCV002625658]\|Odonto-onycho-dermal dysplasia [RCV005398945]	uncertain significance	2	218881033	218881033	Human	2	name
156055767	CV1974562	single nucleotide variant	NM_025216.3(WNT10A):c.37C>T (p.Arg13Ter)	Odonto-onycho-dermal dysplasia [RCV002590808]	pathogenic	2	218881032	218881032	Human	1	name
156333108	CV2000740	single nucleotide variant	NM_025216.3(WNT10A):c.822G>A (p.Lys274=)	Odonto-onycho-dermal dysplasia [RCV002649929]	likely benign	2	218892839	218892839	Human	1	name
156396845	CV2012448	single nucleotide variant	NM_025216.3(WNT10A):c.900C>T (p.Ile300=)	Odonto-onycho-dermal dysplasia [RCV002725628]	likely benign	2	218892917	218892917	Human	1	name
156270683	CV2026916	single nucleotide variant	NM_025216.3(WNT10A):c.441T>C (p.Asn147=)	Odonto-onycho-dermal dysplasia [RCV002746627]	likely benign	2	218890048	218890048	Human	1	name
156228951	CV2027863	single nucleotide variant	NM_025216.3(WNT10A):c.483G>T (p.Ala161=)	Odonto-onycho-dermal dysplasia [RCV002745232]	likely benign	2	218890090	218890090	Human	1	name
156108895	CV2058130	single nucleotide variant	NM_025216.3(WNT10A):c.564G>A (p.Leu188=)	Odonto-onycho-dermal dysplasia [RCV002824842]	likely benign	2	218890171	218890171	Human	1	name
155945159	CV2072563	single nucleotide variant	NM_025216.3(WNT10A):c.840G>T (p.Thr280=)	Odonto-onycho-dermal dysplasia [RCV002862021]	likely benign	2	218892857	218892857	Human	1	name
156110280	CV2077656	single nucleotide variant	NM_025216.3(WNT10A):c.68G>A (p.Trp23Ter)	Odonto-onycho-dermal dysplasia [RCV002889159]	pathogenic	2	218881063	218881063	Human	1	name
156033768	CV2079014	single nucleotide variant	NM_025216.3(WNT10A):c.387G>A (p.Glu129=)	Odonto-onycho-dermal dysplasia [RCV002867160]	likely benign	2	218889994	218889994	Human	1	name
156244787	CV2086151	single nucleotide variant	NM_025216.3(WNT10A):c.918C>T (p.Asn306=)	Odonto-onycho-dermal dysplasia [RCV002876728]	likely benign	2	218892935	218892935	Human	1	name
156105412	CV2096392	single nucleotide variant	NM_025216.3(WNT10A):c.585C>T (p.His195=)	Odonto-onycho-dermal dysplasia [RCV002913564]	likely benign	2	218890192	218890192	Human	1	name
156134992	CV2097312	single nucleotide variant	NM_025216.3(WNT10A):c.612C>A (p.Gly204=)	Odonto-onycho-dermal dysplasia [RCV002890091]	likely benign	2	218890219	218890219	Human	1	name
156231898	CV2156970	single nucleotide variant	NM_025216.3(WNT10A):c.981G>T (p.Pro327=)	Odonto-onycho-dermal dysplasia [RCV003025676]	likely benign	2	218892998	218892998	Human	1	name
156189328	CV2178873	single nucleotide variant	NM_025216.3(WNT10A):c.318C>T (p.Asn106=)	Odonto-onycho-dermal dysplasia [RCV003057782]	likely benign	2	218882365	218882365	Human	1	name
156094949	CV2183467	single nucleotide variant	NM_025216.3(WNT10A):c.903G>A (p.Arg301=)	Odonto-onycho-dermal dysplasia [RCV003054500]	likely benign	2	218892920	218892920	Human	1	name
156191357	CV2206149	single nucleotide variant	NM_057168.2(WNT16):c.190C>T (p.Pro64Ser)	not specified [RCV004078552]	uncertain significance	7	121329661	121329661	Human		name
156266058	CV2275444	single nucleotide variant	NM_057168.2(WNT16):c.266G>A (p.Arg89Lys)	not specified [RCV004135319]	uncertain significance	7	121329737	121329737	Human		name
155902869	CV2356542	single nucleotide variant	NM_057168.2(WNT16):c.261C>G (p.His87Gln)	not specified [RCV004199452]	uncertain significance	7	121329732	121329732	Human		name
329847321	CV2534505	single nucleotide variant	NM_003394.4(WNT10B):c.53T>A (p.Leu18Gln)	Split hand-foot malformation 6 [RCV003228717]	likely pathogenic	12	48970477	48970477	Human	1	name
401866524	CV2782868	single nucleotide variant	NM_057168.2(WNT16):c.283A>G (p.Thr95Ala)	not specified [RCV004361676]	likely benign	7	121329754	121329754	Human		name
401929391	CV2806938	single nucleotide variant	NM_003394.4(WNT10B):c.849C>A (p.Ile283=)	Inborn genetic diseases [RCV004364500]\|not provided [RCV003390221]	likely benign	12	48966416	48966416	Human	1	name
11587954	CV285418	single nucleotide variant	NM_025216.3(WNT10A):c.498C>T (p.Asp166=)	Odonto-onycho-dermal dysplasia [RCV000343294]\|Odonto-onycho-dermal dysplasia [RCV001488558]\|SchC6pf-Schulz-Passarge syndrome [RCV000299178]\|Tooth agenesis, selective, 4 [RCV000396407]	likely benign\|uncertain significance	2	218890105	218890105	Human	3	name
11587416	CV287876	single nucleotide variant	NM_025216.3(WNT10A):c.420C>T (p.Gly140=)	Odonto-onycho-dermal dysplasia [RCV000295107]\|Odonto-onycho-dermal dysplasia [RCV001447441]\|SchC6pf-Schulz-Passarge syndrome [RCV000330331]\|Selective tooth agenesis [RCV000389567]	likely benign	2	218890027	218890027	Human	5	name
405025123	CV3082063	single nucleotide variant	NM_025216.3(WNT10A):c.399C>T (p.Ala133=)	Odonto-onycho-dermal dysplasia [RCV003785669]	likely benign	2	218890006	218890006	Human	1	name
405029218	CV3082428	single nucleotide variant	NM_025216.3(WNT10A):c.405C>T (p.Ala135=)	Odonto-onycho-dermal dysplasia [RCV003785879]	likely benign	2	218890012	218890012	Human	1	name
405011325	CV3083424	single nucleotide variant	NM_025216.3(WNT10A):c.936G>C (p.Pro312=)	Odonto-onycho-dermal dysplasia [RCV003784371]	likely benign	2	218892953	218892953	Human	1	name
405047920	CV3084369	single nucleotide variant	NM_025216.3(WNT10A):c.435G>A (p.Val145=)	Odonto-onycho-dermal dysplasia [RCV003797775]	likely benign	2	218890042	218890042	Human	1	name
402518557	CV3086145	single nucleotide variant	NM_025216.3(WNT10A):c.915C>T (p.Arg305=)	Odonto-onycho-dermal dysplasia [RCV003780916]	likely benign	2	218892932	218892932	Human	1	name
402515341	CV3087634	single nucleotide variant	NM_025216.3(WNT10A):c.981G>A (p.Pro327=)	Odonto-onycho-dermal dysplasia [RCV003789985]\|not provided [RCV004723474]	likely benign	2	218892998	218892998	Human	1	name
402512109	CV3089333	single nucleotide variant	NM_025216.3(WNT10A):c.537G>A (p.Leu179=)	Odonto-onycho-dermal dysplasia [RCV003780365]	likely benign	2	218890144	218890144	Human	1	name
404992516	CV3091414	single nucleotide variant	NM_025216.3(WNT10A):c.858G>C (p.Val286=)	Odonto-onycho-dermal dysplasia [RCV003792889]	likely benign	2	218892875	218892875	Human	1	name
402519657	CV3091874	single nucleotide variant	NM_025216.3(WNT10A):c.741C>T (p.Asn247=)	Odonto-onycho-dermal dysplasia [RCV003790320]	likely benign	2	218890348	218890348	Human	1	name
405012155	CV3093444	single nucleotide variant	NM_025216.3(WNT10A):c.579G>A (p.Pro193=)	Odonto-onycho-dermal dysplasia [RCV003784448]	likely benign	2	218890186	218890186	Human	1	name
402485954	CV3093843	single nucleotide variant	NM_025216.3(WNT10A):c.666G>A (p.Glu222=)	Odonto-onycho-dermal dysplasia [RCV003787044]	likely benign	2	218890273	218890273	Human	1	name
404990262	CV3094647	single nucleotide variant	NM_025216.3(WNT10A):c.927G>A (p.Gln309=)	Odonto-onycho-dermal dysplasia [RCV003792660]	likely benign	2	218892944	218892944	Human	1	name
404990677	CV3094688	single nucleotide variant	NM_025216.3(WNT10A):c.69G>A (p.Trp23Ter)	Odonto-onycho-dermal dysplasia [RCV003792702]	pathogenic	2	218881064	218881064	Human	1	name
405031607	CV3095310	single nucleotide variant	NM_025216.3(WNT10A):c.843C>G (p.Pro281=)	Odonto-onycho-dermal dysplasia [RCV003796516]	likely benign	2	218892860	218892860	Human	1	name
405033037	CV3095402	single nucleotide variant	NM_025216.3(WNT10A):c.966G>A (p.Pro322=)	Odonto-onycho-dermal dysplasia [RCV003796608]	likely benign	2	218892983	218892983	Human	1	name
405004446	CV3095921	single nucleotide variant	NM_025216.3(WNT10A):c.507C>T (p.Ala169=)	Odonto-onycho-dermal dysplasia [RCV003794071]	likely benign	2	218890114	218890114	Human	1	name
405005188	CV3096002	single nucleotide variant	NM_025216.3(WNT10A):c.663G>A (p.Gly221=)	Odonto-onycho-dermal dysplasia [RCV003794152]	likely benign	2	218890270	218890270	Human	1	name
404983733	CV3096375	single nucleotide variant	NM_025216.3(WNT10A):c.795C>T (p.His265=)	Odonto-onycho-dermal dysplasia [RCV003791924]	likely benign	2	218892812	218892812	Human	1	name
405005604	CV3098465	single nucleotide variant	NM_025216.3(WNT10A):c.903G>T (p.Arg301=)	Odonto-onycho-dermal dysplasia [RCV003804396]	likely benign	2	218892920	218892920	Human	1	name
404981009	CV3099688	deletion	NM_025216.3(WNT10A):c.5_27del (p.Gly2fs)	Odonto-onycho-dermal dysplasia [RCV003791517]	pathogenic	2	218880997	218881019	Human	1	name
405079075	CV3100546	single nucleotide variant	NM_025216.3(WNT10A):c.762G>A (p.Val254=)	Odonto-onycho-dermal dysplasia [RCV003800099]	likely benign	2	218892779	218892779	Human	1	name
405018372	CV3100858	single nucleotide variant	NM_025216.3(WNT10A):c.462G>T (p.Leu154=)	Odonto-onycho-dermal dysplasia [RCV003805606]	likely benign	2	218890069	218890069	Human	1	name
405178733	CV3101523	single nucleotide variant	NM_025216.3(WNT10A):c.59C>A (p.Pro20Gln)	Inborn genetic diseases [RCV004968467]\|Odonto-onycho-dermal dysplasia [RCV003803736]	uncertain significance	2	218881054	218881054	Human	2	name
405064375	CV3103119	single nucleotide variant	NM_025216.3(WNT10A):c.720G>T (p.Ala240=)	Odonto-onycho-dermal dysplasia [RCV003799110]	likely benign	2	218890327	218890327	Human	1	name
405170839	CV3104327	single nucleotide variant	NM_025216.3(WNT10A):c.309G>A (p.Gln103=)	Odonto-onycho-dermal dysplasia [RCV003803004]	likely benign	2	218882356	218882356	Human	1	name
405171257	CV3104367	single nucleotide variant	NM_025216.3(WNT10A):c.462G>A (p.Leu154=)	Odonto-onycho-dermal dysplasia [RCV003803044]	likely benign	2	218890069	218890069	Human	1	name
405094035	CV3105503	deletion	NM_025216.3(WNT10A):c.152del (p.Pro51fs)	Odonto-onycho-dermal dysplasia [RCV003801220]	pathogenic	2	218882194	218882194	Human	1	name
405152225	CV3105774	single nucleotide variant	NM_025216.3(WNT10A):c.882C>T (p.Phe294=)	Odonto-onycho-dermal dysplasia [RCV003801491]	likely benign	2	218892899	218892899	Human	1	name
405151665	CV3105783	single nucleotide variant	NM_025216.3(WNT10A):c.576C>G (p.Val192=)	Odonto-onycho-dermal dysplasia [RCV003801500]	likely benign	2	218890183	218890183	Human	1	name
405008780	CV3109007	single nucleotide variant	NM_025216.3(WNT10A):c.801G>T (p.Thr267=)	Odonto-onycho-dermal dysplasia [RCV003804674]	likely benign	2	218892818	218892818	Human	1	name
405155423	CV3111301	single nucleotide variant	NM_025216.3(WNT10A):c.306C>T (p.Asp102=)	Odonto-onycho-dermal dysplasia [RCV003801757]	likely benign	2	218882353	218882353	Human	1	name
405104902	CV3113130	single nucleotide variant	NM_025216.3(WNT10A):c.342C>T (p.Asn114=)	Odonto-onycho-dermal dysplasia [RCV003812421]	likely benign	2	218882389	218882389	Human	1	name
405165429	CV3114091	duplication	NM_025216.3(WNT10A):c.251dup (p.Ala85fs)	Odonto-onycho-dermal dysplasia [RCV003802505]	pathogenic	2	218882297	218882298	Human	1	name
405812105	CV3352915	single nucleotide variant	NM_004626.3(WNT11):c.182G>A (p.Ser61Asn)	not specified [RCV004483115]	uncertain significance	11	76196620	76196620	Human		name
405812111	CV3352918	single nucleotide variant	NM_057168.2(WNT16):c.146A>G (p.Asn49Ser)	not specified [RCV004483118]	uncertain significance	7	121329617	121329617	Human		name
405812113	CV3352919	single nucleotide variant	NM_057168.2(WNT16):c.221C>A (p.Ala74Asp)	not specified [RCV004483119]	uncertain significance	7	121329692	121329692	Human		name
407524810	CV3487975	single nucleotide variant	NM_057168.2(WNT16):c.251A>G (p.Gln84Arg)	not specified [RCV004678566]	uncertain significance	7	121329722	121329722	Human		name
597631062	CV3624200	single nucleotide variant	NM_003394.4(WNT10B):c.55T>A (p.Phe19Ile)	Inborn genetic diseases [RCV004967505]	uncertain significance	12	48970475	48970475	Human	1	name
597740991	CV3624208	single nucleotide variant	NM_057168.2(WNT16):c.113C>T (p.Ser38Phe)	not specified [RCV004890662]	uncertain significance	7	121329584	121329584	Human		name
597741001	CV3624212	single nucleotide variant	NM_057168.2(WNT16):c.283A>T (p.Thr95Ser)	not specified [RCV004890664]	uncertain significance	7	121329754	121329754	Human		name
597875110	CV3747511	single nucleotide variant	NM_003394.4(WNT10B):c.330C>A (p.Leu110=)	not provided [RCV005069195]	likely benign	12	48970096	48970096	Human		name
597871435	CV3866651	single nucleotide variant	NM_025216.3(WNT10A):c.573G>A (p.Gly191=)	Odonto-onycho-dermal dysplasia [RCV005215797]	likely benign	2	218890180	218890180	Human	1	name
597840282	CV3873489	single nucleotide variant	NM_025216.3(WNT10A):c.819C>G (p.Leu273=)	Odonto-onycho-dermal dysplasia [RCV005226316]	likely benign	2	218892836	218892836	Human	1	name
13607896	CV517815	single nucleotide variant	NM_025216.3(WNT10A):c.801G>C (p.Thr267=)	Odonto-onycho-dermal dysplasia [RCV000639739]	likely benign	2	218892818	218892818	Human	1	name
14730488	CV629470	single nucleotide variant	NM_025216.3(WNT10A):c.756G>A (p.Gln252=)	Odonto-onycho-dermal dysplasia [RCV000817424]	uncertain significance	2	218890363	218890363	Human	1	name
15128662	CV691032	single nucleotide variant	NM_025216.3(WNT10A):c.534A>G (p.Gln178=)	Odonto-onycho-dermal dysplasia [RCV000875526]\|Odonto-onycho-dermal dysplasia [RCV001141500]\|SchC6pf-Schulz-Passarge syndrome [RCV001141501]\|Tooth agenesis, selective, 4 [RCV001141502]	benign\|likely benign	2	218890141	218890141	Human	3	name
15109984	CV691033	single nucleotide variant	NM_025216.3(WNT10A):c.660C>T (p.Phe220=)	Odonto-onycho-dermal dysplasia [RCV000872013]\|SchC6pf-Schulz-Passarge syndrome [RCV001271494]	likely benign\|uncertain significance	2	218890267	218890267	Human	3	name
15151045	CV697326	single nucleotide variant	NM_025216.3(WNT10A):c.801G>A (p.Thr267=)	Odonto-onycho-dermal dysplasia [RCV000945611]\|SchC6pf-Schulz-Passarge syndrome [RCV001277357]\|not provided [RCV004711438]	likely benign\|uncertain significance	2	218892818	218892818	Human	3	name
15126633	CV733172	single nucleotide variant	NM_025216.3(WNT10A):c.429C>T (p.His143=)	Odonto-onycho-dermal dysplasia [RCV001503184]\|SchC6pf-Schulz-Passarge syndrome [RCV001830957]	likely benign	2	218890036	218890036	Human	3	name
15138307	CV733173	single nucleotide variant	NM_025216.3(WNT10A):c.732T>G (p.Leu244=)	Odonto-onycho-dermal dysplasia [RCV000898957]	likely benign	2	218890339	218890339	Human	1	name
15128719	CV747302	single nucleotide variant	NM_025216.3(WNT10A):c.444G>A (p.Ala148=)	Odonto-onycho-dermal dysplasia [RCV000919702]\|SchC6pf-Schulz-Passarge syndrome [RCV001271493]	likely benign\|uncertain significance	2	218890051	218890051	Human	3	name
15106855	CV747303	single nucleotide variant	NM_025216.3(WNT10A):c.591C>T (p.Ala197=)	Odonto-onycho-dermal dysplasia [RCV000915837]\|SchC6pf-Schulz-Passarge syndrome [RCV001836012]	benign	2	218890198	218890198	Human	3	name
15101077	CV747304	single nucleotide variant	NM_025216.3(WNT10A):c.864G>A (p.Ala288=)	Odonto-onycho-dermal dysplasia [RCV002540878]	likely benign	2	218892881	218892881	Human	1	name
15115296	CV753401	single nucleotide variant	NM_003394.4(WNT10B):c.498A>C (p.Ala166=)	not provided [RCV000917430]	likely benign	12	48968159	48968159	Human		name
15098687	CV762937	single nucleotide variant	NM_025216.3(WNT10A):c.390C>T (p.Ser130=)	Odonto-onycho-dermal dysplasia [RCV000936334]	likely benign	2	218889997	218889997	Human	1	name
15191962	CV762938	single nucleotide variant	NM_025216.3(WNT10A):c.495G>C (p.Gly165=)	Odonto-onycho-dermal dysplasia [RCV001492338]	likely benign	2	218890102	218890102	Human	1	name
15189320	CV762939	single nucleotide variant	NM_025216.3(WNT10A):c.570T>C (p.His190=)	Odonto-onycho-dermal dysplasia [RCV001476023]	likely benign	2	218890177	218890177	Human	1	name
15124349	CV762940	single nucleotide variant	NM_025216.3(WNT10A):c.705C>T (p.His235=)	Odonto-onycho-dermal dysplasia [RCV001409139]	likely benign	2	218890312	218890312	Human	1	name
15185416	CV762941	single nucleotide variant	NM_025216.3(WNT10A):c.744A>G (p.Arg248=)	Odonto-onycho-dermal dysplasia [RCV001465383]	likely benign	2	218890351	218890351	Human	1	name
15191140	CV762942	single nucleotide variant	NM_025216.3(WNT10A):c.771C>T (p.Asn257=)	Odonto-onycho-dermal dysplasia [RCV000932718]	likely benign	2	218892788	218892788	Human	1	name
15177527	CV762943	single nucleotide variant	NM_025216.3(WNT10A):c.906G>T (p.Pro302=)	Odonto-onycho-dermal dysplasia [RCV001493973]	likely benign	2	218892923	218892923	Human	1	name
15196481	CV762944	single nucleotide variant	NM_025216.3(WNT10A):c.969C>A (p.Gly323=)	Odonto-onycho-dermal dysplasia [RCV001467606]	likely benign	2	218892986	218892986	Human	1	name
15119044	CV781182	single nucleotide variant	NM_025216.3(WNT10A):c.642C>T (p.Cys214=)	Odonto-onycho-dermal dysplasia [RCV000979053]	likely benign	2	218890249	218890249	Human	1	name
15111498	CV781183	single nucleotide variant	NM_025216.3(WNT10A):c.825G>T (p.Thr275=)	Odonto-onycho-dermal dysplasia [RCV001443633]	likely benign	2	218892842	218892842	Human	1	name
15132398	CV781185	single nucleotide variant	NM_025216.3(WNT10A):c.957G>T (p.Ser319=)	Odonto-onycho-dermal dysplasia [RCV000981375]\|SchC6pf-Schulz-Passarge syndrome [RCV001832284]	likely benign	2	218892974	218892974	Human	3	name
8627292	CV82436	single nucleotide variant	NM_003394.3(WNT10B):c.699G>A (p.Arg233=)	Malignant melanoma [RCV000062515]	not provided	12	48967958	48967958	Human		name
28882552	CV883766	single nucleotide variant	NM_025216.3(WNT10A):c.483G>C (p.Ala161=)	Odonto-onycho-dermal dysplasia [RCV001143236]\|Odonto-onycho-dermal dysplasia [RCV001403230]\|SchC6pf-Schulz-Passarge syndrome [RCV001143237]\|Tooth agenesis, selective, 4 [RCV001136662]	likely benign\|uncertain significance	2	218890090	218890090	Human	3	name
8634378	CV89598	single nucleotide variant	NM_004626.2(WNT11):c.278C>T (p.Ser93Phe)	Malignant melanoma [RCV000069695]	not provided	11	76196524	76196524	Human		name
127236221	CV1059193	deletion	NM_025216.3(WNT10A):c.648del (p.Asp217fs)	Odonto-onycho-dermal dysplasia [RCV001382570]	pathogenic	2	218890252	218890252	Human	1	name
127255567	CV1059196	deletion	NM_025216.3(WNT10A):c.932del (p.Glu311fs)	Odonto-onycho-dermal dysplasia [RCV001386374]	pathogenic	2	218892949	218892949	Human	1	name
127267628	CV1059197	duplication	NM_025216.3(WNT10A):c.932dup (p.Pro312fs)	Odonto-onycho-dermal dysplasia [RCV001389023]\|not provided [RCV004801005]	pathogenic\|likely pathogenic	2	218892948	218892949	Human	1	name
127263468	CV1059199	deletion	NM_025216.3(WNT10A):c.993del (p.Ser332fs)	Odonto-onycho-dermal dysplasia [RCV001387962]	pathogenic	2	218893009	218893009	Human	1	name
127274801	CV1069108	single nucleotide variant	NM_025216.3(WNT10A):c.1131C>T (p.Cys377=)	Odonto-onycho-dermal dysplasia [RCV001406458]	likely benign	2	218893148	218893148	Human	1	name
127231109	CV1069109	single nucleotide variant	NM_025216.3(WNT10A):c.1149C>T (p.Ile383=)	Odonto-onycho-dermal dysplasia [RCV001395129]	likely benign	2	218893166	218893166	Human	1	name
127279247	CV1069110	single nucleotide variant	NM_025216.3(WNT10A):c.1251G>A (p.Lys417=)	Odonto-onycho-dermal dysplasia [RCV001408963]	likely benign	2	218893268	218893268	Human	1	name
127256967	CV1090799	single nucleotide variant	NM_025216.3(WNT10A):c.1044C>A (p.Arg348=)	Odonto-onycho-dermal dysplasia [RCV001437817]	likely benign	2	218893061	218893061	Human	1	name
127280311	CV1090800	single nucleotide variant	NM_025216.3(WNT10A):c.1047G>A (p.Glu349=)	Odonto-onycho-dermal dysplasia [RCV001446372]	likely benign	2	218893064	218893064	Human	1	name
127275407	CV1090801	single nucleotide variant	NM_025216.3(WNT10A):c.1116C>T (p.Cys372=)	Odonto-onycho-dermal dysplasia [RCV001443314]	likely benign	2	218893133	218893133	Human	1	name
127275536	CV1090802	single nucleotide variant	NM_025216.3(WNT10A):c.1161G>T (p.Thr387=)	Odonto-onycho-dermal dysplasia [RCV001443363]	likely benign	2	218893178	218893178	Human	1	name
127233654	CV1090803	single nucleotide variant	NM_025216.3(WNT10A):c.1221C>T (p.Cys407=)	Odonto-onycho-dermal dysplasia [RCV001421828]	likely benign	2	218893238	218893238	Human	1	name
127315217	CV1112316	single nucleotide variant	NM_025216.3(WNT10A):c.1002C>T (p.Ala334=)	Odonto-onycho-dermal dysplasia [RCV001457933]	likely benign	2	218893019	218893019	Human	1	name
127302546	CV1112317	single nucleotide variant	NM_025216.3(WNT10A):c.1098C>T (p.Ser366=)	Odonto-onycho-dermal dysplasia [RCV001461664]	likely benign	2	218893115	218893115	Human	1	name
127307748	CV1112318	single nucleotide variant	NM_025216.3(WNT10A):c.1107G>T (p.Ser369=)	Odonto-onycho-dermal dysplasia [RCV001455857]	likely benign	2	218893124	218893124	Human	1	name
127295260	CV1112319	single nucleotide variant	NM_025216.3(WNT10A):c.1146C>T (p.Asn382=)	Odonto-onycho-dermal dysplasia [RCV001459699]\|SchC6pf-Schulz-Passarge syndrome [RCV001832599]	likely benign	2	218893163	218893163	Human	3	name
127299691	CV1112320	single nucleotide variant	NM_025216.3(WNT10A):c.1158G>A (p.Gln386=)	Odonto-onycho-dermal dysplasia [RCV001453647]	likely benign	2	218893175	218893175	Human	1	name
127328208	CV1112321	single nucleotide variant	NM_025216.3(WNT10A):c.1161G>A (p.Thr387=)	Odonto-onycho-dermal dysplasia [RCV001469473]	likely benign	2	218893178	218893178	Human	1	name
127288558	CV1133218	single nucleotide variant	NM_025216.3(WNT10A):c.125A>G (p.Asn42Ser)	Odonto-onycho-dermal dysplasia [RCV001495286]\|SchC6pf-Schulz-Passarge syndrome [RCV001826330]	likely benign	2	218882172	218882172	Human	3	name
127305726	CV1133234	single nucleotide variant	NM_025216.3(WNT10A):c.1092G>A (p.Lys364=)	Odonto-onycho-dermal dysplasia [RCV001479827]	likely benign	2	218893109	218893109	Human	1	name
127287367	CV1133235	single nucleotide variant	NM_025216.3(WNT10A):c.1107G>A (p.Ser369=)	Odonto-onycho-dermal dysplasia [RCV001494895]	likely benign	2	218893124	218893124	Human	1	name
127288578	CV1133236	single nucleotide variant	NM_025216.3(WNT10A):c.1140C>T (p.Gly380=)	Odonto-onycho-dermal dysplasia [RCV001495298]	likely benign	2	218893157	218893157	Human	1	name
127285854	CV1133237	single nucleotide variant	NM_025216.3(WNT10A):c.1143C>T (p.His381=)	Odonto-onycho-dermal dysplasia [RCV001493767]	likely benign	2	218893160	218893160	Human	1	name
150335022	CV1164419	single nucleotide variant	NM_003394.4(WNT10B):c.1059C>T (p.His353=)	Split hand-foot malformation 6 [RCV002243291]\|Tooth agenesis, selective, 8 [RCV002243292]\|not provided [RCV001707877]\|not specified [RCV001530025]	benign	12	48966206	48966206	Human	2	name
150487658	CV1208139	single nucleotide variant	NM_003394.4(WNT10B):c.229C>T (p.His77Tyr)	not provided [RCV001591999]	conflicting interpretations of pathogenicity\|uncertain significance	12	48970197	48970197	Human		name
150520609	CV1289672	single nucleotide variant	NM_025216.3(WNT10A):c.262G>A (p.Gly88Ser)	Tooth agenesis, selective, 4 [RCV001730091]	uncertain significance	2	218882309	218882309	Human	1	name
151662631	CV1330567	single nucleotide variant	NM_004626.3(WNT11):c.922A>G (p.Ser308Gly)	Hypospadias [RCV001824104]	uncertain significance	11	76187208	76187208	Human	2	name
151856686	CV1377377	deletion	NM_025216.3(WNT10A):c.580del (p.Glu194fs)	Odonto-onycho-dermal dysplasia [RCV001923484]	pathogenic	2	218890186	218890186	Human	1	name
152087595	CV1536431	single nucleotide variant	NM_025216.3(WNT10A):c.1128C>T (p.Cys376=)	Odonto-onycho-dermal dysplasia [RCV002171391]	likely benign	2	218893145	218893145	Human	1	name
152050873	CV1596658	single nucleotide variant	NM_025216.3(WNT10A):c.1050G>T (p.Pro350=)	Odonto-onycho-dermal dysplasia [RCV002166863]	likely benign	2	218893067	218893067	Human	1	name
152035503	CV1604184	single nucleotide variant	NM_025216.3(WNT10A):c.1006C>T (p.Leu336=)	Odonto-onycho-dermal dysplasia [RCV002087139]	likely benign	2	218893023	218893023	Human	1	name
152103843	CV1614403	single nucleotide variant	NM_025216.3(WNT10A):c.1011C>A (p.Val337=)	Odonto-onycho-dermal dysplasia [RCV002079331]	likely benign	2	218893028	218893028	Human	1	name
152042367	CV1618039	single nucleotide variant	NM_025216.3(WNT10A):c.1239C>A (p.Val413=)	Odonto-onycho-dermal dysplasia [RCV002206515]	likely benign	2	218893256	218893256	Human	1	name
152053386	CV1619393	single nucleotide variant	NM_025216.3(WNT10A):c.1170G>A (p.Glu390=)	Odonto-onycho-dermal dysplasia [RCV002167148]	likely benign	2	218893187	218893187	Human	1	name
152173327	CV1637797	single nucleotide variant	NM_025216.3(WNT10A):c.1023G>A (p.Lys341=)	Odonto-onycho-dermal dysplasia [RCV002162769]	likely benign	2	218893040	218893040	Human	1	name
152111722	CV1640440	single nucleotide variant	NM_025216.3(WNT10A):c.1164C>T (p.Arg388=)	Odonto-onycho-dermal dysplasia [RCV002174421]	likely benign	2	218893181	218893181	Human	1	name
156050832	CV1869025	single nucleotide variant	NM_003394.4(WNT10B):c.1062C>T (p.Asn354=)	not provided [RCV003052993]	likely benign	12	48966203	48966203	Human		name
10046770	CV187239	single nucleotide variant	NM_004626.3(WNT11):c.947G>A (p.Arg316His)	Bladder exstrophy-epispadias-cloacal extrophy complex [RCV000172903]	uncertain significance	11	76187183	76187183	Human	1	name
156409299	CV1873952	single nucleotide variant	NM_025216.3(WNT10A):c.1080C>A (p.Arg360=)	Odonto-onycho-dermal dysplasia [RCV003071615]	likely benign	2	218893097	218893097	Human	1	name
155973763	CV1889738	single nucleotide variant	NM_025216.3(WNT10A):c.274G>A (p.Ala92Thr)	Odonto-onycho-dermal dysplasia [RCV003075306]	likely pathogenic\|uncertain significance	2	218882321	218882321	Human	1	name
156418373	CV1911020	single nucleotide variant	NM_025216.3(WNT10A):c.1110T>C (p.Asp370=)	Odonto-onycho-dermal dysplasia [RCV002611559]	likely benign	2	218893127	218893127	Human	1	name
155953404	CV1918235	single nucleotide variant	NM_025216.3(WNT10A):c.1101C>G (p.Ala367=)	Odonto-onycho-dermal dysplasia [RCV002616346]	likely benign	2	218893118	218893118	Human	1	name
156142924	CV1918236	single nucleotide variant	NM_025216.3(WNT10A):c.1137C>T (p.Arg379=)	Odonto-onycho-dermal dysplasia [RCV002623726]	likely benign	2	218893154	218893154	Human	1	name
156444019	CV1941298	single nucleotide variant	NM_025216.3(WNT10A):c.1059C>T (p.Asp353=)	Odonto-onycho-dermal dysplasia [RCV003114935]	likely benign	2	218893076	218893076	Human	1	name
156202373	CV2010993	single nucleotide variant	NM_025216.3(WNT10A):c.1188C>T (p.Phe396=)	Odonto-onycho-dermal dysplasia [RCV002700323]	likely benign	2	218893205	218893205	Human	1	name
156304567	CV2013648	single nucleotide variant	NM_025216.3(WNT10A):c.1242C>T (p.Ser414=)	Odonto-onycho-dermal dysplasia [RCV002716215]	likely benign	2	218893259	218893259	Human	1	name
156260561	CV2033944	single nucleotide variant	NM_025216.3(WNT10A):c.1056G>A (p.Leu352=)	Odonto-onycho-dermal dysplasia [RCV002746293]	likely benign	2	218893073	218893073	Human	1	name
156225279	CV2085528	deletion	NM_025216.3(WNT10A):c.574del (p.Val192fs)	Odonto-onycho-dermal dysplasia [RCV002894342]	pathogenic	2	218890178	218890178	Human	1	name
156256067	CV2090052	deletion	NM_025216.3(WNT10A):c.673del (p.Ser225fs)	Odonto-onycho-dermal dysplasia [RCV002877108]	pathogenic	2	218890277	218890277	Human	1	name
156317026	CV2104238	single nucleotide variant	NM_025216.3(WNT10A):c.152C>T (p.Pro51Leu)	Inborn genetic diseases [RCV004966167]\|Odonto-onycho-dermal dysplasia [RCV002937512]	uncertain significance	2	218882199	218882199	Human	2	name
155955560	CV2143969	deletion	NM_025216.3(WNT10A):c.386del (p.Glu129fs)	Odonto-onycho-dermal dysplasia [RCV002994875]	pathogenic	2	218889993	218889993	Human	1	name
156250411	CV2157467	single nucleotide variant	NM_025216.3(WNT10A):c.1212C>T (p.Cys404=)	Odonto-onycho-dermal dysplasia [RCV003008423]	likely benign	2	218893229	218893229	Human	1	name
156328306	CV2161118	single nucleotide variant	NM_025216.3(WNT10A):c.1185C>T (p.Arg395=)	Odonto-onycho-dermal dysplasia [RCV003029618]	likely benign	2	218893202	218893202	Human	1	name
156197169	CV2186767	single nucleotide variant	NM_025216.3(WNT10A):c.1197C>T (p.Cys399=)	Odonto-onycho-dermal dysplasia [RCV003058034]	likely benign	2	218893214	218893214	Human	1	name
156105397	CV2217586	single nucleotide variant	NM_004626.3(WNT11):c.749G>A (p.Arg250Gln)	not specified [RCV004090112]	uncertain significance	11	76191705	76191705	Human		name
156364024	CV2262757	single nucleotide variant	NM_003394.4(WNT10B):c.287C>A (p.Ala96Glu)	Inborn genetic diseases [RCV002813262]	uncertain significance	12	48970139	48970139	Human	1	name
156164413	CV2270264	single nucleotide variant	NM_025216.3(WNT10A):c.192G>C (p.Leu64Phe)	Inborn genetic diseases [RCV002827591]	uncertain significance	2	218882239	218882239	Human	1	name
156095808	CV2310133	single nucleotide variant	NM_057168.2(WNT16):c.878A>C (p.Tyr293Ser)	not specified [RCV004163252]	uncertain significance	7	121339125	121339125	Human		name
156390648	CV2383284	single nucleotide variant	NM_057168.2(WNT16):c.682G>A (p.Gly228Ser)	not specified [RCV004222332]	uncertain significance	7	121338929	121338929	Human		name
156190463	CV2384996	single nucleotide variant	NM_004626.3(WNT11):c.719G>A (p.Arg240Gln)	not specified [RCV004228268]	uncertain significance	11	76191735	76191735	Human		name
156051569	CV2386372	single nucleotide variant	NM_003394.4(WNT10B):c.241C>G (p.His81Asp)	Inborn genetic diseases [RCV002704977]	uncertain significance	12	48970185	48970185	Human	1	name
156093130	CV2389662	single nucleotide variant	NM_057168.2(WNT16):c.863A>G (p.Asn288Ser)	not specified [RCV004243716]	uncertain significance	7	121339110	121339110	Human		name
243051552	CV2403926	single nucleotide variant	NM_025216.3(WNT10A):c.131T>C (p.Ile44Thr)	not provided [RCV003128995]	uncertain significance	2	218882178	218882178	Human		name
329393381	CV2449692	single nucleotide variant	NM_004626.3(WNT11):c.754A>C (p.Met252Leu)	not specified [RCV004268595]	uncertain significance	11	76191700	76191700	Human		name
329369130	CV2450537	single nucleotide variant	NM_004626.3(WNT11):c.799C>A (p.Pro267Thr)	not specified [RCV004265447]	uncertain significance	11	76191655	76191655	Human		name
329378218	CV2459040	single nucleotide variant	NM_057168.2(WNT16):c.757T>C (p.Tyr253His)	not specified [RCV004272512]	uncertain significance	7	121339004	121339004	Human		name
329397887	CV2464105	single nucleotide variant	NM_004626.3(WNT11):c.925T>A (p.Cys309Ser)	not specified [RCV004273801]	uncertain significance	11	76187205	76187205	Human		name
11633364	CV264061	duplication	NM_025216.3(WNT10A):c.985dup (p.Arg329fs)	not provided [RCV000332548]	pathogenic	2	218893000	218893001	Human		name
401726652	CV2677297	single nucleotide variant	NM_057168.2(WNT16):c.568A>T (p.Thr190Ser)	not specified [RCV004295915]	uncertain significance	7	121331899	121331899	Human		name
401758251	CV2678290	single nucleotide variant	NM_003394.4(WNT10B):c.190C>T (p.Arg64Cys)	Inborn genetic diseases [RCV003279644]	uncertain significance	12	48970236	48970236	Human	1	name
401733301	CV2685486	single nucleotide variant	NM_004626.3(WNT11):c.451G>A (p.Gly151Arg)	not specified [RCV004294508]	uncertain significance	11	76194713	76194713	Human		name
401757404	CV2692982	single nucleotide variant	NM_057168.2(WNT16):c.736G>A (p.Gly246Ser)	not specified [RCV004306494]	uncertain significance	7	121338983	121338983	Human		name
401737838	CV2700735	single nucleotide variant	NM_004626.3(WNT11):c.427G>C (p.Val143Leu)	not specified [RCV004307026]	uncertain significance	11	76194737	76194737	Human		name
401719232	CV2701001	single nucleotide variant	NM_057168.2(WNT16):c.802C>T (p.Arg268Cys)	not specified [RCV004309613]	uncertain significance	7	121339049	121339049	Human		name
401751701	CV2706722	single nucleotide variant	NM_004626.3(WNT11):c.661C>A (p.Arg221Ser)	not specified [RCV004319286]	uncertain significance	11	76191793	76191793	Human		name
401738130	CV2714335	single nucleotide variant	NM_004626.3(WNT11):c.568C>T (p.Arg190Cys)	not specified [RCV004317876]	uncertain significance	11	76194596	76194596	Human		name
401763525	CV2714583	single nucleotide variant	NM_057168.2(WNT16):c.598G>A (p.Ala200Thr)	not specified [RCV004318092]	uncertain significance	7	121331929	121331929	Human		name
401828803	CV2743138	single nucleotide variant	NM_003394.4(WNT10B):c.265G>A (p.Asp89Asn)	not provided [RCV003325847]	uncertain significance	12	48970161	48970161	Human		name
401866684	CV2758970	single nucleotide variant	NM_004626.3(WNT11):c.919G>A (p.Asp307Asn)	not specified [RCV004342284]	uncertain significance	11	76187211	76187211	Human		name
401895062	CV2792754	single nucleotide variant	NM_003394.4(WNT10B):c.100C>G (p.Leu34Val)	Inborn genetic diseases [RCV003372152]	uncertain significance	12	48970326	48970326	Human	1	name
401948070	CV2832171	single nucleotide variant	NM_003394.4(WNT10B):c.115G>T (p.Glu39Ter)	Split hand-foot malformation 6 [RCV003447696]	likely pathogenic	12	48970311	48970311	Human	1	name
11578777	CV284741	single nucleotide variant	NM_025216.3(WNT10A):c.149C>T (p.Pro50Leu)	Odonto-onycho-dermal dysplasia [RCV000344076]\|Odonto-onycho-dermal dysplasia [RCV000543463]\|SchC6pf-Schulz-Passarge syndrome [RCV000289030]\|Tooth agenesis, selective, 4 [RCV000397838]	likely benign\|uncertain significance	2	218882196	218882196	Human	3	name
11588549	CV285422	single nucleotide variant	NM_025216.3(WNT10A):c.1017C>T (p.Phe339=)	Odonto-onycho-dermal dysplasia [RCV000303716]\|Odonto-onycho-dermal dysplasia [RCV000873083]\|SchC6pf-Schulz-Passarge syndrome [RCV000358475]\|Tooth agenesis, selective, 4 [RCV000400970]	likely benign\|uncertain significance	2	218893034	218893034	Human	3	name
11650224	CV287902	single nucleotide variant	NM_025216.3(WNT10A):c.1134C>T (p.Gly378=)	Odonto-onycho-dermal dysplasia [RCV000327060]\|Odonto-onycho-dermal dysplasia [RCV002057663]\|SchC6pf-Schulz-Passarge syndrome [RCV000291835]\|Tooth agenesis, selective, 4 [RCV000383955]	likely benign\|uncertain significance	2	218893151	218893151	Human	3	name
405024393	CV3085048	single nucleotide variant	NM_025216.3(WNT10A):c.1041G>A (p.Glu347=)	Odonto-onycho-dermal dysplasia [RCV003795914]	likely benign	2	218893058	218893058	Human	1	name
402515352	CV3087635	single nucleotide variant	NM_025216.3(WNT10A):c.1167C>T (p.Ser389=)	Odonto-onycho-dermal dysplasia [RCV003789986]	likely benign	2	218893184	218893184	Human	1	name
404985908	CV3096815	single nucleotide variant	NM_025216.3(WNT10A):c.1101C>A (p.Ala367=)	Odonto-onycho-dermal dysplasia [RCV003792204]	likely benign	2	218893118	218893118	Human	1	name
405036035	CV3098858	deletion	NM_025216.3(WNT10A):c.380del (p.Phe127fs)	Odonto-onycho-dermal dysplasia [RCV003806984]	pathogenic	2	218889985	218889985	Human	1	name
405095172	CV3105600	single nucleotide variant	NM_025216.3(WNT10A):c.1053C>G (p.Arg351=)	Odonto-onycho-dermal dysplasia [RCV003801317]	likely benign	2	218893070	218893070	Human	1	name
405009217	CV3105982	single nucleotide variant	NM_025216.3(WNT10A):c.1179C>T (p.His393=)	Odonto-onycho-dermal dysplasia [RCV003794480]	likely benign	2	218893196	218893196	Human	1	name
405166931	CV3107180	single nucleotide variant	NM_025216.3(WNT10A):c.1011C>T (p.Val337=)	Odonto-onycho-dermal dysplasia [RCV003802671]	likely benign	2	218893028	218893028	Human	1	name
405082151	CV3107456	single nucleotide variant	NM_025216.3(WNT10A):c.1206G>C (p.Val402=)	Odonto-onycho-dermal dysplasia [RCV003800326]	likely benign	2	218893223	218893223	Human	1	name
405064511	CV3108882	duplication	NM_025216.3(WNT10A):c.694dup (p.Arg232fs)	Odonto-onycho-dermal dysplasia [RCV003809292]	pathogenic	2	218890298	218890299	Human	1	name
405125896	CV3111887	single nucleotide variant	NM_025216.3(WNT10A):c.1155C>T (p.Arg385=)	Odonto-onycho-dermal dysplasia [RCV003815360]	likely benign	2	218893172	218893172	Human	1	name
405109200	CV3112466	single nucleotide variant	NM_025216.3(WNT10A):c.1218G>A (p.Glu406=)	Odonto-onycho-dermal dysplasia [RCV003813309]	likely benign	2	218893235	218893235	Human	1	name
405124352	CV3113461	single nucleotide variant	NM_025216.3(WNT10A):c.1081C>T (p.Leu361=)	Odonto-onycho-dermal dysplasia [RCV003815217]	likely benign	2	218893098	218893098	Human	1	name
405004524	CV3120824	single nucleotide variant	NM_003394.4(WNT10B):c.105G>T (p.Lys35Asn)	not provided [RCV003828427]	uncertain significance	12	48970321	48970321	Human		name
404991755	CV3132308	duplication	NM_003394.4(WNT10B):c.969dup (p.Met324fs)	not provided [RCV003827246]	pathogenic	12	48966295	48966296	Human		name
405812091	CV3352908	single nucleotide variant	NM_025216.3(WNT10A):c.200T>C (p.Leu67Pro)	Inborn genetic diseases [RCV004483108]\|not provided [RCV005230629]	uncertain significance	2	218882247	218882247	Human	1	name
405812093	CV3352909	single nucleotide variant	NM_025216.3(WNT10A):c.230G>A (p.Arg77His)	Inborn genetic diseases [RCV004483109]	uncertain significance	2	218882277	218882277	Human	1	name
405812109	CV3352917	single nucleotide variant	NM_004626.3(WNT11):c.962A>G (p.Tyr321Cys)	not specified [RCV004483117]	uncertain significance	11	76187168	76187168	Human		name
405812115	CV3352920	single nucleotide variant	NM_057168.2(WNT16):c.452C>T (p.Thr151Ile)	not specified [RCV004483120]	uncertain significance	7	121331783	121331783	Human		name
405812117	CV3352921	single nucleotide variant	NM_057168.2(WNT16):c.688T>A (p.Cys230Ser)	not specified [RCV004483121]	uncertain significance	7	121338935	121338935	Human		name
405812118	CV3352922	single nucleotide variant	NM_057168.2(WNT16):c.949G>A (p.Ala317Thr)	not specified [RCV004483122]	uncertain significance	7	121339196	121339196	Human		name
407428635	CV3410307	single nucleotide variant	NM_025216.3(WNT10A):c.206G>A (p.Arg69Gln)	not specified [RCV004587914]	uncertain significance	2	218882253	218882253	Human		name
407524790	CV3487966	single nucleotide variant	NM_003394.4(WNT10B):c.209C>T (p.Ala70Val)	Inborn genetic diseases [RCV004678558]	uncertain significance	12	48970217	48970217	Human	1	name
407524796	CV3487969	single nucleotide variant	NM_004626.3(WNT11):c.971G>A (p.Arg324His)	not specified [RCV004678561]	uncertain significance	11	76187159	76187159	Human		name
407465493	CV3487970	single nucleotide variant	NM_004626.3(WNT11):c.983G>A (p.Arg328Gln)	not specified [RCV004688783]	uncertain significance	11	76187147	76187147	Human		name
407524805	CV3487973	single nucleotide variant	NM_057168.2(WNT16):c.743T>G (p.Leu248Trp)	not specified [RCV004678564]	uncertain significance	7	121338990	121338990	Human		name
408390501	CV3519389	single nucleotide variant	NM_025216.3(WNT10A):c.152C>G (p.Pro51Arg)	not provided [RCV004762698]	uncertain significance	2	218882199	218882199	Human		name
596920575	CV3534049	single nucleotide variant	NM_025216.3(WNT10A):c.286T>C (p.Cys96Arg)	not specified [RCV004783267]	uncertain significance	2	218882333	218882333	Human		name
596928070	CV3541269	deletion	NM_003394.4(WNT10B):c.523del (p.His175fs)	Split hand-foot malformation 6 [RCV004797140]	likely pathogenic	12	48968134	48968134	Human	1	name
597631056	CV3624197	single nucleotide variant	NM_003394.4(WNT10B):c.284C>A (p.Ser95Tyr)	Inborn genetic diseases [RCV004967502]	uncertain significance	12	48970142	48970142	Human	1	name
597631060	CV3624199	single nucleotide variant	NM_003394.4(WNT10B):c.139G>T (p.Val47Leu)	Inborn genetic diseases [RCV004967504]	uncertain significance	12	48970287	48970287	Human	1	name
597799986	CV3624202	single nucleotide variant	NM_004626.3(WNT11):c.383G>A (p.Arg128Gln)	not specified [RCV004879967]	uncertain significance	11	76194781	76194781	Human		name
597799988	CV3624203	single nucleotide variant	NM_004626.3(WNT11):c.728C>T (p.Ser243Leu)	not specified [RCV004879968]	uncertain significance	11	76191726	76191726	Human		name
597799989	CV3624204	single nucleotide variant	NM_004626.3(WNT11):c.820G>A (p.Val274Ile)	not specified [RCV004879969]	uncertain significance	11	76191634	76191634	Human		name
597740982	CV3624205	single nucleotide variant	NM_004626.3(WNT11):c.458G>A (p.Arg153His)	not specified [RCV004890660]	uncertain significance	11	76194706	76194706	Human		name
597799991	CV3624206	single nucleotide variant	NM_004626.3(WNT11):c.604C>A (p.Arg202Ser)	not specified [RCV004879970]	uncertain significance	11	76191850	76191850	Human		name
597740996	CV3624209	single nucleotide variant	NM_057168.2(WNT16):c.713C>A (p.Thr238Asn)	not specified [RCV004890663]	uncertain significance	7	121338960	121338960	Human		name
597799993	CV3624210	single nucleotide variant	NM_057168.2(WNT16):c.994C>T (p.His332Tyr)	not specified [RCV004879971]	uncertain significance	7	121339241	121339241	Human		name
597799997	CV3624213	single nucleotide variant	NM_057168.2(WNT16):c.794G>A (p.Arg265Lys)	not specified [RCV004879973]	uncertain significance	7	121339041	121339041	Human		name
597763251	CV3706109	single nucleotide variant	NM_025216.3(WNT10A):c.293A>C (p.His98Pro)	Odonto-onycho-dermal dysplasia [RCV005018651]	uncertain significance	2	218882340	218882340	Human	1	name
597920111	CV3865424	deletion	NM_025216.3(WNT10A):c.812del (p.Cys271fs)	Odonto-onycho-dermal dysplasia [RCV005223368]	pathogenic	2	218892829	218892829	Human	1	name
597851035	CV3873345	single nucleotide variant	NM_025216.3(WNT10A):c.262G>T (p.Gly88Cys)	Odonto-onycho-dermal dysplasia [RCV005212787]	uncertain significance	2	218882309	218882309	Human	1	name
597860532	CV3874807	single nucleotide variant	NM_025216.3(WNT10A):c.259C>T (p.Gln87Ter)	Odonto-onycho-dermal dysplasia [RCV005214148]	pathogenic	2	218882306	218882306	Human	1	name
598236062	CV3937158	single nucleotide variant	NM_003394.4(WNT10B):c.222G>C (p.Gln74His)	Inborn genetic diseases [RCV005295954]	uncertain significance	12	48970204	48970204	Human	1	name
598236070	CV3937160	single nucleotide variant	NM_004626.3(WNT11):c.406C>A (p.Pro136Thr)	not specified [RCV005295956]	uncertain significance	11	76194758	76194758	Human		name
598236076	CV3937161	single nucleotide variant	NM_004626.3(WNT11):c.332C>T (p.Ser111Leu)	not specified [RCV005295957]	uncertain significance	11	76194832	76194832	Human		name
598236082	CV3937162	single nucleotide variant	NM_004626.3(WNT11):c.736A>G (p.Lys246Glu)	not specified [RCV005295958]	uncertain significance	11	76191718	76191718	Human		name
598275512	CV3937164	single nucleotide variant	NM_004626.3(WNT11):c.607G>A (p.Ala203Thr)	not specified [RCV005304646]	uncertain significance	11	76191847	76191847	Human		name
598236092	CV3937165	single nucleotide variant	NM_004626.3(WNT11):c.532G>A (p.Val178Met)	not specified [RCV005295960]	uncertain significance	11	76194632	76194632	Human		name
598192239	CV3937167	single nucleotide variant	NM_057168.2(WNT16):c.492C>A (p.His164Gln)	not specified [RCV005288487]	uncertain significance	7	121331823	121331823	Human		name
598275513	CV3937168	single nucleotide variant	NM_057168.2(WNT16):c.313G>A (p.Ala105Thr)	not specified [RCV005304647]	likely benign	7	121329784	121329784	Human		name
12900840	CV405617	single nucleotide variant	NM_025216.3(WNT10A):c.242T>C (p.Val81Ala)	not provided [RCV000483296]	uncertain significance	2	218882289	218882289	Human		name
13493382	CV450625	single nucleotide variant	NM_025216.3(WNT10A):c.216G>T (p.Met72Ile)	Inborn genetic diseases [RCV005298518]\|Odonto-onycho-dermal dysplasia [RCV000558141]\|SchC6pf-Schulz-Passarge syndrome [RCV001829581]	uncertain significance	2	218882263	218882263	Human	4	name
13607900	CV517833	single nucleotide variant	NM_025216.3(WNT10A):c.275C>T (p.Ala92Val)	Inborn genetic diseases [RCV004025588]\|Odonto-onycho-dermal dysplasia [RCV000639736]	uncertain significance	2	218882322	218882322	Human	2	name
13790558	CV550121	deletion	NM_025216.3(WNT10A):c.949del (p.Ala317fs)	Odonto-onycho-dermal dysplasia [RCV000677103]\|Odonto-onycho-dermal dysplasia [RCV001868287]	pathogenic\|likely pathogenic	2	218892962	218892962	Human	1	name
13801286	CV559115	single nucleotide variant	NM_025216.3(WNT10A):c.212A>T (p.Gln71Leu)	Odonto-onycho-dermal dysplasia [RCV000697721]	uncertain significance	2	218882259	218882259	Human	1	name
14396548	CV612296	single nucleotide variant	NM_003394.4(WNT10B):c.290T>C (p.Leu97Pro)	Split hand-foot malformation 6 [RCV000761463]	uncertain significance	12	48970136	48970136	Human	1	name
14696332	CV622517	deletion	NM_003394.4(WNT10B):c.817del (p.Ala273fs)	Split hand-foot malformation 6 [RCV000785180]	pathogenic	12	48966448	48966448	Human	1	name
14696334	CV622518	duplication	NM_003394.4(WNT10B):c.817dup (p.Ala273fs)	Split hand-foot malformation 6 [RCV000785182]\|Tooth agenesis, selective, 8 [RCV001253087]	pathogenic\|uncertain significance	12	48966447	48966448	Human	2	name
25327361	CV625985	single nucleotide variant	NM_003394.4(WNT10B):c.257A>C (p.Gln86Pro)	Split hand-foot malformation 6 [RCV001027401]	likely pathogenic	12	48970169	48970169	Human	1	name
14703100	CV629469	deletion	NM_025216.3(WNT10A):c.694del (p.Arg232fs)	Odonto-onycho-dermal dysplasia [RCV000792132]\|Odonto-onycho-dermal dysplasia [RCV002290429]\|Odonto-onycho-dermal dysplasia [RCV002507361]\|not provided [RCV001784406]	pathogenic\|likely pathogenic	2	218890299	218890299	Human	1	name
14711700	CV629471	duplication	NM_025216.3(WNT10A):c.949dup (p.Ala317fs)	Odonto-onycho-dermal dysplasia [RCV000818549]	pathogenic	2	218892961	218892962	Human	1	name
15185946	CV699784	single nucleotide variant	NM_057168.2(WNT16):c.778T>C (p.Ser260Pro)	not provided [RCV000953135]	benign	7	121339025	121339025	Human		name
15134964	CV713186	single nucleotide variant	NM_004626.3(WNT11):c.361G>A (p.Ala121Thr)	not provided [RCV000965210]	benign	11	76194803	76194803	Human		name
15199849	CV753402	single nucleotide variant	NM_003394.4(WNT10B):c.110C>G (p.Pro37Arg)	not provided [RCV000912672]	benign	12	48970316	48970316	Human		name
15121310	CV762945	single nucleotide variant	NM_025216.3(WNT10A):c.1005C>T (p.Asp335=)	Odonto-onycho-dermal dysplasia [RCV000940498]\|SchC6pf-Schulz-Passarge syndrome [RCV001832146]\|not provided [RCV004711432]	likely benign	2	218893022	218893022	Human	3	name
15147523	CV762946	single nucleotide variant	NM_025216.3(WNT10A):c.1044C>G (p.Arg348=)	Odonto-onycho-dermal dysplasia [RCV001468079]	likely benign	2	218893061	218893061	Human	1	name
15184661	CV762947	single nucleotide variant	NM_025216.3(WNT10A):c.1173C>T (p.Arg391=)	Odonto-onycho-dermal dysplasia [RCV001488970]	likely benign	2	218893190	218893190	Human	1	name
26886237	CV825745	deletion	NM_025216.3(WNT10A):c.717del (p.His239fs)	Odonto-onycho-dermal dysplasia [RCV001044079]	pathogenic	2	218890324	218890324	Human	1	name
28882186	CV883763	single nucleotide variant	NM_025216.3(WNT10A):c.166A>G (p.Asn56Asp)	Odonto-onycho-dermal dysplasia [RCV001136563]\|SchC6pf-Schulz-Passarge syndrome [RCV001136561]\|Tooth agenesis, selective, 4 [RCV001136562]	uncertain significance	2	218882213	218882213	Human	3	name
126747059	CV1017616	single nucleotide variant	NM_003394.4(WNT10B):c.505C>T (p.Arg169Ter)	Split-hand/foot malformation 6 [RCV001331051]	pathogenic	12	48968152	48968152	Human		name
126773693	CV1024150	single nucleotide variant	NM_025216.3(WNT10A):c.519G>T (p.Lys173Asn)	Odonto-onycho-dermal dysplasia [RCV001346367]\|SchC6pf-Schulz-Passarge syndrome [RCV001825929]	uncertain significance	2	218890126	218890126	Human	3	name
127272888	CV1059187	microsatellite	NM_025216.3(WNT10A):c.55_56dup (p.Pro20fs)	Odonto-onycho-dermal dysplasia [RCV001390604]	pathogenic	2	218881047	218881048	Human		name
127266405	CV1059190	single nucleotide variant	NM_025216.3(WNT10A):c.315G>A (p.Trp105Ter)	Odonto-onycho-dermal dysplasia [RCV001388708]	pathogenic	2	218882362	218882362	Human	1	name
127266803	CV1059191	single nucleotide variant	NM_025216.3(WNT10A):c.490C>T (p.Arg164Ter)	Odonto-onycho-dermal dysplasia [RCV001388812]	pathogenic	2	218890097	218890097	Human	1	name
127262138	CV1059194	single nucleotide variant	NM_025216.3(WNT10A):c.832C>T (p.Gln278Ter)	Odonto-onycho-dermal dysplasia [RCV001387650]\|Odonto-onycho-dermal dysplasia [RCV005014540]	pathogenic\|likely pathogenic	2	218892849	218892849	Human	1	name
127248459	CV1090794	single nucleotide variant	NM_025216.3(WNT10A):c.745G>A (p.Val249Ile)	Odonto-onycho-dermal dysplasia [RCV001435834]\|SchC6pf-Schulz-Passarge syndrome [RCV001826250]	likely benign	2	218890352	218890352	Human	3	name
127275063	CV1090798	single nucleotide variant	NM_025216.3(WNT10A):c.902G>C (p.Arg301Pro)	Odonto-onycho-dermal dysplasia [RCV001443172]	likely benign	2	218892919	218892919	Human	1	name
127330830	CV1133226	single nucleotide variant	NM_025216.3(WNT10A):c.514A>T (p.Arg172Trp)	Odonto-onycho-dermal dysplasia [RCV001488387]\|not provided [RCV003222327]	likely benign\|uncertain significance	2	218890121	218890121	Human	1	name
150333748	CV1164187	single nucleotide variant	NM_025216.3(WNT10A):c.347T>C (p.Ile116Thr)	Odonto-onycho-dermal dysplasia [RCV002476846]\|Odonto-onycho-dermal dysplasia [RCV002568872]\|not provided [RCV001529084]	likely benign\|uncertain significance	2	218882394	218882394	Human	1	name
150334436	CV1164188	single nucleotide variant	NM_025216.3(WNT10A):c.831G>C (p.Trp277Cys)	not provided [RCV001529617]	pathogenic\|likely pathogenic	2	218892848	218892848	Human		name
150548753	CV1294492	single nucleotide variant	NM_025216.3(WNT10A):c.937G>C (p.Gly313Arg)	not provided [RCV001751984]	uncertain significance	2	218892954	218892954	Human		name
150552916	CV1295590	single nucleotide variant	NM_025216.3(WNT10A):c.430G>C (p.Ala144Pro)	not provided [RCV001768522]	uncertain significance	2	218890037	218890037	Human		name
150555444	CV1297915	single nucleotide variant	NM_025216.3(WNT10A):c.862G>A (p.Ala288Thr)	Inborn genetic diseases [RCV005288535]\|not provided [RCV001772823]	uncertain significance	2	218892879	218892879	Human	1	name
150543900	CV1309863	single nucleotide variant	NM_025216.3(WNT10A):c.318C>G (p.Asn106Lys)	Odonto-onycho-dermal dysplasia [RCV003772103]\|not provided [RCV003237607]	likely pathogenic\|uncertain significance	2	218882365	218882365	Human	1	name
151795457	CV1338611	single nucleotide variant	NM_025216.3(WNT10A):c.623C>T (p.Ser208Phe)	Odonto-onycho-dermal dysplasia [RCV001898571]	uncertain significance	2	218890230	218890230	Human	1	name
151725134	CV1356464	duplication	NM_025216.3(WNT10A):c.1091dup (p.Ser365fs)	Odonto-onycho-dermal dysplasia [RCV001910237]	pathogenic	2	218893106	218893107	Human	1	name
151816811	CV1388482	single nucleotide variant	NM_025216.3(WNT10A):c.670T>C (p.Phe224Leu)	Odonto-onycho-dermal dysplasia [RCV001992375]	uncertain significance	2	218890277	218890277	Human	1	name
151886109	CV1428672	single nucleotide variant	NM_025216.3(WNT10A):c.354T>A (p.Tyr118Ter)	Odonto-onycho-dermal dysplasia [RCV002037900]	pathogenic	2	218882401	218882401	Human	1	name
151713617	CV1451104	single nucleotide variant	NM_025216.3(WNT10A):c.627G>A (p.Trp209Ter)	Odonto-onycho-dermal dysplasia [RCV002002481]\|Tooth agenesis, selective, 4 [RCV003223745]\|not provided [RCV003130636]	pathogenic\|likely pathogenic	2	218890234	218890234	Human	2	name
151738395	CV1455053	single nucleotide variant	NM_025216.3(WNT10A):c.322T>C (p.Ser108Pro)	Odonto-onycho-dermal dysplasia [RCV002005566]\|Odonto-onycho-dermal dysplasia [RCV005017009]	likely pathogenic	2	218882369	218882369	Human	1	name
151876379	CV1461386	single nucleotide variant	NM_025216.3(WNT10A):c.914G>T (p.Arg305Leu)	Odonto-onycho-dermal dysplasia [RCV001925868]	uncertain significance	2	218892931	218892931	Human	1	name
151836101	CV1471639	deletion	NM_025216.3(WNT10A):c.1063del (p.Ala355fs)	Odonto-onycho-dermal dysplasia [RCV001956186]	pathogenic	2	218893079	218893079	Human	1	name
151867955	CV1516554	single nucleotide variant	NM_025216.3(WNT10A):c.323C>T (p.Ser108Leu)	Odonto-onycho-dermal dysplasia [RCV001980937]	uncertain significance	2	218882370	218882370	Human	1	name
153000875	CV1683899	single nucleotide variant	NM_025216.3(WNT10A):c.877C>T (p.Arg293Cys)	Abnormality of the dentition [RCV002254493]	uncertain significance	2	218892894	218892894	Human	1	name
153301859	CV1689344	single nucleotide variant	NM_003394.4(WNT10B):c.343C>G (p.Arg115Gly)	not provided [RCV002267294]	uncertain significance	12	48968314	48968314	Human		name
155267755	CV1699173	single nucleotide variant	NM_025216.3(WNT10A):c.985C>T (p.Arg329Ter)	Tooth agenesis, selective, 4 [RCV002282968]	uncertain significance	2	218893002	218893002	Human	1	name
155268896	CV1705722	single nucleotide variant	NM_025216.3(WNT10A):c.812G>A (p.Cys271Tyr)	Tooth agenesis, selective, 4 [RCV002286330]	likely pathogenic	2	218892829	218892829	Human	1	name
156052725	CV1867764	single nucleotide variant	NM_025216.3(WNT10A):c.353A>G (p.Tyr118Cys)	Tooth agenesis, selective, 4 [RCV002510236]	likely pathogenic	2	218882400	218882400	Human	1	name
156403200	CV1904412	single nucleotide variant	NM_025216.3(WNT10A):c.434T>C (p.Val145Ala)	Odonto-onycho-dermal dysplasia [RCV002585162]	uncertain significance	2	218890041	218890041	Human	1	name
8558098	CV19499	single nucleotide variant	NM_025216.3(WNT10A):c.697G>T (p.Glu233Ter)	Odonto-onycho-dermal dysplasia [RCV000004714]\|Odonto-onycho-dermal dysplasia [RCV001851651]	pathogenic	2	218890304	218890304	Human	1	name
8558101	CV19502	single nucleotide variant	NM_025216.3(WNT10A):c.383G>A (p.Arg128Gln)	Odonto-onycho-dermal dysplasia [RCV000004718]\|Odonto-onycho-dermal dysplasia [RCV000824631]\|Odonto-onycho-dermal dysplasia [RCV005016239]\|Tooth agenesis, selective, 4 [RCV000030651]\|not provided [RCV000059803]	pathogenic\|likely pathogenic\|not provided	2	218889990	218889990	Human	2	name
155963420	CV1952202	single nucleotide variant	NM_003394.4(WNT10B):c.337G>C (p.Gly113Arg)	Split hand-foot malformation 6 [RCV002512480]	uncertain significance	12	48970089	48970089	Human	1	name
156380412	CV1964237	single nucleotide variant	NM_003394.4(WNT10B):c.818C>T (p.Ala273Val)	Inborn genetic diseases [RCV004064449]\|not provided [RCV002583128]	uncertain significance	12	48966447	48966447	Human	1	name
156340672	CV1984862	single nucleotide variant	NM_003394.4(WNT10B):c.542G>A (p.Gly181Asp)	not provided [RCV002631417]	benign	12	48968115	48968115	Human		name
156127598	CV2005510	single nucleotide variant	NM_003394.4(WNT10B):c.832C>T (p.Arg278Trp)	not provided [RCV002663096]	uncertain significance	12	48966433	48966433	Human		name
155902748	CV2010290	single nucleotide variant	NM_025216.3(WNT10A):c.775C>T (p.Arg259Trp)	Odonto-onycho-dermal dysplasia [RCV002726286]	uncertain significance	2	218892792	218892792	Human	1	name
155944646	CV2039512	single nucleotide variant	NM_003394.4(WNT10B):c.893G>A (p.Arg298His)	not provided [RCV002775408]	uncertain significance	12	48966372	48966372	Human		name
156309390	CV2082085	deletion	NM_025216.3(WNT10A):c.1046del (p.Glu349fs)	Odonto-onycho-dermal dysplasia [RCV002898625]	pathogenic	2	218893063	218893063	Human	1	name
156313017	CV2107696	single nucleotide variant	NM_025216.3(WNT10A):c.662G>T (p.Gly221Val)	Odonto-onycho-dermal dysplasia [RCV002937282]	likely pathogenic	2	218890269	218890269	Human	1	name
156296330	CV2119255	single nucleotide variant	NM_003394.4(WNT10B):c.854T>C (p.Ile285Thr)	not provided [RCV002961935]	conflicting interpretations of pathogenicity	12	48966411	48966411	Human		name
155959684	CV2131718	single nucleotide variant	NM_003394.4(WNT10B):c.967A>C (p.Thr323Pro)	Inborn genetic diseases [RCV002995094]\|not provided [RCV002995093]	likely benign\|uncertain significance	12	48966298	48966298	Human	1	name
156104497	CV2139828	single nucleotide variant	NM_003394.4(WNT10B):c.391G>A (p.Ala131Thr)	Inborn genetic diseases [RCV005301215]\|not provided [RCV003002342]	uncertain significance	12	48968266	48968266	Human	1	name
156347220	CV2191310	single nucleotide variant	NM_025216.3(WNT10A):c.532C>T (p.Gln178Ter)	Odonto-onycho-dermal dysplasia [RCV003048075]	pathogenic	2	218890139	218890139	Human	1	name
156248303	CV2192622	single nucleotide variant	NM_003394.4(WNT10B):c.767G>A (p.Cys256Tyr)	not provided [RCV003059926]	likely pathogenic\|uncertain significance	12	48966498	48966498	Human		name
156167933	CV2237274	single nucleotide variant	NM_003394.4(WNT10B):c.523C>G (p.His175Asp)	Inborn genetic diseases [RCV002787891]	uncertain significance	12	48968134	48968134	Human	1	name
8597603	CV22669	single nucleotide variant	NM_003394.4(WNT10B):c.994C>T (p.Arg332Trp)	Split hand-foot malformation 6 [RCV000008069]\|not provided [RCV003555964]	pathogenic	12	48966271	48966271	Human	1	name
155924642	CV2277156	single nucleotide variant	NM_003394.4(WNT10B):c.539C>T (p.Pro180Leu)	Inborn genetic diseases [RCV002860146]	uncertain significance	12	48968118	48968118	Human	1	name
156007759	CV2288357	single nucleotide variant	NM_057168.2(WNT16):c.1009G>A (p.Val337Met)	not specified [RCV004150125]	uncertain significance	7	121339256	121339256	Human		name
156004668	CV2290208	single nucleotide variant	NM_025216.3(WNT10A):c.715C>T (p.His239Tyr)	Inborn genetic diseases [RCV002883567]	uncertain significance	2	218890322	218890322	Human	1	name
155930502	CV2296929	single nucleotide variant	NM_003394.4(WNT10B):c.700G>A (p.Val234Met)	Inborn genetic diseases [RCV002860900]	uncertain significance	12	48967957	48967957	Human	1	name
156245269	CV2310322	single nucleotide variant	NM_025216.3(WNT10A):c.692C>T (p.Ser231Phe)	Inborn genetic diseases [RCV002919576]	uncertain significance	2	218890299	218890299	Human	1	name
156290438	CV2324906	single nucleotide variant	NM_003394.4(WNT10B):c.913T>C (p.Ser305Pro)	Inborn genetic diseases [RCV002935567]	uncertain significance	12	48966352	48966352	Human	1	name
156072285	CV2325314	single nucleotide variant	NM_003394.4(WNT10B):c.725A>C (p.Asn242Thr)	Inborn genetic diseases [RCV002925687]	uncertain significance	12	48966540	48966540	Human	1	name
156203794	CV2331516	single nucleotide variant	NM_025216.3(WNT10A):c.946G>A (p.Gly316Arg)	Inborn genetic diseases [RCV002931761]\|not provided [RCV004593194]	uncertain significance	2	218892963	218892963	Human	1	name
156131990	CV2365664	single nucleotide variant	NM_025216.3(WNT10A):c.779G>A (p.Arg260Gln)	Inborn genetic diseases [RCV002981906]\|Odonto-onycho-dermal dysplasia [RCV005227860]\|not provided [RCV004798030]	uncertain significance	2	218892796	218892796	Human	2	name
155930172	CV2366585	single nucleotide variant	NM_003394.4(WNT10B):c.892C>T (p.Arg298Cys)	Inborn genetic diseases [RCV002993164]	uncertain significance	12	48966373	48966373	Human	1	name
155904535	CV2385534	single nucleotide variant	NM_025216.3(WNT10A):c.712A>C (p.Ile238Leu)	Inborn genetic diseases [RCV002749236]	uncertain significance	2	218890319	218890319	Human	1	name
243062088	CV2414294	single nucleotide variant	NM_025216.3(WNT10A):c.980C>A (p.Pro327Gln)	not provided [RCV003139363]	uncertain significance	2	218892997	218892997	Human		name
329369978	CV2424932	single nucleotide variant	NM_003394.4(WNT10B):c.821C>A (p.Ala274Glu)	Inborn genetic diseases [RCV003184015]	uncertain significance	12	48966444	48966444	Human	1	name
329392618	CV2439072	single nucleotide variant	NM_003394.4(WNT10B):c.841C>T (p.Arg281Trp)	Inborn genetic diseases [RCV003192756]\|not provided [RCV005101282]	uncertain significance	12	48966424	48966424	Human	1	name
329369423	CV2450638	single nucleotide variant	NM_004626.3(WNT11):c.1049G>A (p.Arg350His)	not specified [RCV004265529]	uncertain significance	11	76187081	76187081	Human		name
11531365	CV247468	single nucleotide variant	NM_003394.4(WNT10B):c.632G>A (p.Arg211Gln)	Tooth agenesis, selective, 8 [RCV000239578]	pathogenic	12	48968025	48968025	Human	1	name
11531309	CV247469	single nucleotide variant	NM_003394.4(WNT10B):c.786G>A (p.Trp262Ter)	Tooth agenesis, selective, 8 [RCV000239472]	pathogenic	12	48966479	48966479	Human	1	name
329847165	CV2534324	single nucleotide variant	NM_025216.3(WNT10A):c.684T>G (p.Phe228Leu)	not provided [RCV003228533]	uncertain significance	2	218890291	218890291	Human		name
11559710	CV259730	single nucleotide variant	NM_025216.3(WNT10A):c.391G>A (p.Ala131Thr)	Odonto-onycho-dermal dysplasia [RCV000804067]\|Odonto-onycho-dermal dysplasia [RCV002494800]\|SchC6pf-Schulz-Passarge syndrome [RCV001814131]\|Tooth agenesis, selective, 4 [RCV005252845]\|not provided [RCV000254796]	pathogenic\|likely pathogenic	2	218889998	218889998	Human	3	name
11559968	CV259732	single nucleotide variant	NM_025216.3(WNT10A):c.803C>G (p.Ser268Ter)	Odonto-onycho-dermal dysplasia [RCV001855007]\|Odonto-onycho-dermal dysplasia [RCV002503967]\|not provided [RCV000255393]	pathogenic	2	218892820	218892820	Human	1	name
329955080	CV2671021	single nucleotide variant	NM_025216.3(WNT10A):c.499G>C (p.Glu167Gln)	not specified [RCV003236290]	uncertain significance	2	218890106	218890106	Human		name
401756969	CV2692733	single nucleotide variant	NM_025216.3(WNT10A):c.853A>G (p.Thr285Ala)	Inborn genetic diseases [RCV003255874]	likely benign	2	218892870	218892870	Human	1	name
401778115	CV2700623	single nucleotide variant	NM_003394.4(WNT10B):c.811G>C (p.Val271Leu)	Inborn genetic diseases [RCV003286957]	uncertain significance	12	48966454	48966454	Human	1	name
401763319	CV2714510	single nucleotide variant	NM_025216.3(WNT10A):c.758C>T (p.Ala253Val)	Inborn genetic diseases [RCV003258172]	uncertain significance	2	218892775	218892775	Human	1	name
401799317	CV2741881	single nucleotide variant	NM_025216.3(WNT10A):c.521T>C (p.Leu174Pro)	Odonto-onycho-dermal dysplasia [RCV003327602]\|Tooth agenesis, selective, 4 [RCV003323313]	likely pathogenic	2	218890128	218890128	Human	2	name
401797184	CV2741923	single nucleotide variant	NM_025216.3(WNT10A):c.310C>A (p.Arg104Ser)	Tooth agenesis, selective, 4 [RCV003324102]	uncertain significance	2	218882357	218882357	Human	1	name
401797099	CV2741927	single nucleotide variant	NM_025216.3(WNT10A):c.889G>A (p.Ala297Thr)	Odonto-onycho-dermal dysplasia [RCV005419614]\|Tooth agenesis, selective, 4 [RCV003324106]	likely pathogenic	2	218892906	218892906	Human	2	name
401797186	CV2741928	deletion	NM_025216.3(WNT10A):c.1036del (p.Cys346fs)	Odonto-onycho-dermal dysplasia [RCV003777344]\|Tooth agenesis, selective, 4 [RCV003324107]	pathogenic\|likely pathogenic	2	218893053	218893053	Human	2	name
401829786	CV2747561	single nucleotide variant	NM_003394.4(WNT10B):c.515G>A (p.Ser172Asn)	not provided [RCV003329027]	uncertain significance	12	48968142	48968142	Human		name
401897530	CV2787137	single nucleotide variant	NM_003394.4(WNT10B):c.833G>T (p.Arg278Leu)	Inborn genetic diseases [RCV003375178]	uncertain significance	12	48966432	48966432	Human	1	name
401896821	CV2788818	single nucleotide variant	NM_003394.4(WNT10B):c.733C>T (p.Arg245Trp)	Inborn genetic diseases [RCV003374438]	uncertain significance	12	48966532	48966532	Human	1	name
11578157	CV284752	single nucleotide variant	NM_025216.3(WNT10A):c.349C>T (p.Pro117Ser)	Odonto-onycho-dermal dysplasia [RCV000356033]\|SchC6pf-Schulz-Passarge syndrome [RCV000315891]\|Tooth agenesis, selective, 4 [RCV000275342]	uncertain significance	2	218882396	218882396	Human	3	name
11578690	CV284757	single nucleotide variant	NM_025216.3(WNT10A):c.652A>G (p.Met218Val)	Inborn genetic diseases [RCV002521394]\|Odonto-onycho-dermal dysplasia [RCV000341862]\|Odonto-onycho-dermal dysplasia [RCV002523113]\|SchC6pf-Schulz-Passarge syndrome [RCV000376761]\|Tooth agenesis, selective, 4 [RCV000287049]\|not provided [RCV001814148]	likely benign\|uncertain significance	2	218890259	218890259	Human	4	name
11644543	CV285417	single nucleotide variant	NM_025216.3(WNT10A):c.315G>C (p.Trp105Cys)	Odonto-onycho-dermal dysplasia [RCV000305206]\|SchC6pf-Schulz-Passarge syndrome [RCV000260696]\|Tooth agenesis, selective, 4 [RCV000359992]	uncertain significance	2	218882362	218882362	Human	3	name
11585414	CV285421	single nucleotide variant	NM_025216.3(WNT10A):c.841C>G (p.Pro281Ala)	Inborn genetic diseases [RCV003243092]\|Odonto-onycho-dermal dysplasia [RCV000280724]\|SchC6pf-Schulz-Passarge syndrome [RCV000386136]\|Tooth agenesis, selective, 4 [RCV000350216]	likely benign\|uncertain significance	2	218892858	218892858	Human	4	name
11586941	CV287882	single nucleotide variant	NM_025216.3(WNT10A):c.437C>G (p.Ser146Cys)	Odonto-onycho-dermal dysplasia [RCV000381373]\|SchC6pf-Schulz-Passarge syndrome [RCV000326647]\|Tooth agenesis, selective, 4 [RCV000291690]	uncertain significance	2	218890044	218890044	Human	3	name
11584390	CV287883	single nucleotide variant	NM_025216.3(WNT10A):c.551G>A (p.Arg184His)	Odonto-onycho-dermal dysplasia [RCV000314527]\|Odonto-onycho-dermal dysplasia [RCV002488718]\|Odonto-onycho-dermal dysplasia [RCV002521393]\|SchC6pf-Schulz-Passarge syndrome [RCV000273430]\|Tooth agenesis, selective, 4 [RCV000367917]	likely benign\|uncertain significance	2	218890158	218890158	Human	3	name
11645192	CV287889	single nucleotide variant	NM_025216.3(WNT10A):c.838A>T (p.Thr280Ser)	Odonto-onycho-dermal dysplasia [RCV000263980]\|SchC6pf-Schulz-Passarge syndrome [RCV000378470]\|Tooth agenesis, selective, 4 [RCV000323835]	uncertain significance	2	218892855	218892855	Human	3	name
11582593	CV287891	single nucleotide variant	NM_025216.3(WNT10A):c.841C>A (p.Pro281Thr)	Inborn genetic diseases [RCV000623795]\|Odonto-onycho-dermal dysplasia [RCV000260783]\|SchC6pf-Schulz-Passarge syndrome [RCV000315988]\|Tooth agenesis, selective, 4 [RCV000375200]	uncertain significance	2	218892858	218892858	Human	4	name
405043982	CV3074302	single nucleotide variant	NM_003394.4(WNT10B):c.623A>G (p.Lys208Arg)	not provided [RCV003740128]	likely benign	12	48968034	48968034	Human		name
405237802	CV3077764	single nucleotide variant	NM_003394.4(WNT10B):c.683G>A (p.Arg228Gln)	not provided [RCV003736236]	likely benign	12	48967974	48967974	Human		name
402508713	CV3088834	single nucleotide variant	NM_025216.3(WNT10A):c.547C>T (p.Gln183Ter)	Odonto-onycho-dermal dysplasia [RCV003780038]	pathogenic	2	218890154	218890154	Human	1	name
405035804	CV3093187	single nucleotide variant	NM_025216.3(WNT10A):c.919G>C (p.Gly307Arg)	Odonto-onycho-dermal dysplasia [RCV003786538]	uncertain significance	2	218892936	218892936	Human	1	name
404983235	CV3096315	single nucleotide variant	NM_025216.3(WNT10A):c.542C>T (p.Ala181Val)	Odonto-onycho-dermal dysplasia [RCV003791864]	uncertain significance	2	218890149	218890149	Human	1	name
405176513	CV3101169	single nucleotide variant	NM_025216.3(WNT10A):c.640T>C (p.Cys214Arg)	Odonto-onycho-dermal dysplasia [RCV003803556]	uncertain significance	2	218890247	218890247	Human	1	name
405001599	CV3101824	single nucleotide variant	NM_025216.3(WNT10A):c.813C>A (p.Cys271Ter)	Odonto-onycho-dermal dysplasia [RCV003804038]	pathogenic	2	218892830	218892830	Human	1	name
405003228	CV3102148	single nucleotide variant	NM_025216.3(WNT10A):c.844G>T (p.Glu282Ter)	Odonto-onycho-dermal dysplasia [RCV003804194]	pathogenic	2	218892861	218892861	Human	1	name
405107119	CV3113759	single nucleotide variant	NM_025216.3(WNT10A):c.956C>A (p.Ser319Ter)	Odonto-onycho-dermal dysplasia [RCV003812882]	pathogenic	2	218892973	218892973	Human	1	name
405047604	CV3150718	single nucleotide variant	NM_003394.4(WNT10B):c.836T>C (p.Leu279Pro)	not provided [RCV003849321]	uncertain significance	12	48966429	48966429	Human		name
405812095	CV3352910	single nucleotide variant	NM_025216.3(WNT10A):c.729G>C (p.Arg243Ser)	Inborn genetic diseases [RCV004483110]	uncertain significance	2	218890336	218890336	Human	1	name
405812099	CV3352912	single nucleotide variant	NM_025216.3(WNT10A):c.929T>G (p.Leu310Arg)	Inborn genetic diseases [RCV004483112]	uncertain significance	2	218892946	218892946	Human	1	name
405812101	CV3352913	single nucleotide variant	NM_025216.3(WNT10A):c.967G>A (p.Gly323Ser)	Inborn genetic diseases [RCV004483113]	uncertain significance	2	218892984	218892984	Human	1	name
405812103	CV3352914	single nucleotide variant	NM_003394.4(WNT10B):c.319A>G (p.Ser107Gly)	Inborn genetic diseases [RCV004483114]	uncertain significance	12	48970107	48970107	Human	1	name
405853372	CV3392703	single nucleotide variant	NM_025216.3(WNT10A):c.311G>C (p.Arg104Pro)	not specified [RCV004526428]	uncertain significance	2	218882358	218882358	Human		name
407465488	CV3487960	single nucleotide variant	NM_025216.3(WNT10A):c.789G>C (p.Lys263Asn)	Inborn genetic diseases [RCV004688781]	uncertain significance	2	218892806	218892806	Human	1	name
407524780	CV3487961	single nucleotide variant	NM_025216.3(WNT10A):c.320G>A (p.Cys107Tyr)	Inborn genetic diseases [RCV004678554]	uncertain significance	2	218882367	218882367	Human	1	name
407524783	CV3487962	single nucleotide variant	NM_025216.3(WNT10A):c.599C>G (p.Thr200Arg)	Inborn genetic diseases [RCV004678555]	uncertain significance	2	218890206	218890206	Human	1	name
407524787	CV3487964	single nucleotide variant	NM_003394.4(WNT10B):c.344G>A (p.Arg115Gln)	Inborn genetic diseases [RCV004678557]	uncertain significance	12	48968313	48968313	Human	1	name
407465490	CV3487965	single nucleotide variant	NM_003394.4(WNT10B):c.631C>T (p.Arg211Trp)	Inborn genetic diseases [RCV004688782]	uncertain significance	12	48968026	48968026	Human	1	name
407524792	CV3487967	single nucleotide variant	NM_003394.4(WNT10B):c.533C>T (p.Pro178Leu)	Inborn genetic diseases [RCV004678559]	uncertain significance	12	48968124	48968124	Human	1	name
407524794	CV3487968	single nucleotide variant	NM_003394.4(WNT10B):c.847A>G (p.Ile283Val)	Inborn genetic diseases [RCV004678560]	uncertain significance	12	48966418	48966418	Human	1	name
408382210	CV3525609	single nucleotide variant	NM_025216.3(WNT10A):c.409G>A (p.Ala137Thr)	not specified [RCV004766518]	uncertain significance	2	218890016	218890016	Human		name
408382601	CV3525690	single nucleotide variant	NM_025216.3(WNT10A):c.827G>T (p.Cys276Phe)	not specified [RCV004766600]	uncertain significance	2	218892844	218892844	Human		name
596923457	CV3535789	single nucleotide variant	NM_003394.4(WNT10B):c.343C>T (p.Arg115Ter)	Split hand-foot malformation 6 [RCV004788219]	pathogenic	12	48968314	48968314	Human	1	name
616937627	CV3542518	single nucleotide variant	NM_025216.3(WNT10A):c.354T>G (p.Tyr118Ter)	Tooth agenesis, selective, 4 [RCV005411273]	likely pathogenic	2	218882401	218882401	Human	1	name
596939041	CV3550258	single nucleotide variant	NM_003394.4(WNT10B):c.638T>G (p.Phe213Cys)	Split hand-foot malformation 6 [RCV004813560]	likely pathogenic	12	48968019	48968019	Human	1	name
12739015	CV360835	single nucleotide variant	NM_025216.3(WNT10A):c.667C>T (p.Arg223Cys)	Odonto-onycho-dermal dysplasia [RCV000528997]\|Palmoplantar keratoderma [RCV000415098]\|SchC6pf-Schulz-Passarge syndrome [RCV001828389]\|not provided [RCV004591142]	uncertain significance	2	218890274	218890274	Human	8	name
597631044	CV3624189	single nucleotide variant	NM_025216.3(WNT10A):c.667C>A (p.Arg223Ser)	Inborn genetic diseases [RCV004967496]\|Odonto-onycho-dermal dysplasia [RCV005221157]	uncertain significance	2	218890274	218890274	Human	2	name
597631048	CV3624191	single nucleotide variant	NM_025216.3(WNT10A):c.802T>C (p.Ser268Pro)	Inborn genetic diseases [RCV004967498]	uncertain significance	2	218892819	218892819	Human	1	name
597631050	CV3624192	single nucleotide variant	NM_003394.4(WNT10B):c.805C>T (p.Arg269Trp)	Inborn genetic diseases [RCV004967499]	uncertain significance	12	48966460	48966460	Human	1	name
597631052	CV3624195	single nucleotide variant	NM_003394.4(WNT10B):c.386T>C (p.Met129Thr)	Inborn genetic diseases [RCV004967500]	uncertain significance	12	48968271	48968271	Human	1	name
597631054	CV3624196	single nucleotide variant	NM_003394.4(WNT10B):c.774C>G (p.Phe258Leu)	Inborn genetic diseases [RCV004967501]	uncertain significance	12	48966491	48966491	Human	1	name
597631058	CV3624198	single nucleotide variant	NM_003394.4(WNT10B):c.548G>A (p.Gly183Asp)	Inborn genetic diseases [RCV004967503]	uncertain significance	12	48968109	48968109	Human	1	name
597631064	CV3624201	single nucleotide variant	NM_003394.4(WNT10B):c.755C>T (p.Thr252Ile)	Inborn genetic diseases [RCV004967506]	uncertain significance	12	48966510	48966510	Human	1	name
597740986	CV3624207	single nucleotide variant	NM_057168.2(WNT16):c.1052G>A (p.Arg351His)	not specified [RCV004890661]	uncertain significance	7	121339299	121339299	Human		name
12849512	CV367004	single nucleotide variant	NM_025216.3(WNT10A):c.650A>G (p.Asp217Gly)	Odonto-onycho-dermal dysplasia [RCV005222923]\|not provided [RCV000431228]\|not specified [RCV005418111]	pathogenic\|uncertain significance	2	218890257	218890257	Human	1	name
597763256	CV3706110	single nucleotide variant	NM_025216.3(WNT10A):c.376G>A (p.Gly126Ser)	Odonto-onycho-dermal dysplasia [RCV005018652]	likely pathogenic	2	218882423	218882423	Human	1	name
597882947	CV3865959	deletion	NM_025216.3(WNT10A):c.1141del (p.His381fs)	Odonto-onycho-dermal dysplasia [RCV005217624]	pathogenic	2	218893157	218893157	Human	1	name
597837172	CV3866753	single nucleotide variant	NM_025216.3(WNT10A):c.898A>T (p.Ile300Phe)	Odonto-onycho-dermal dysplasia [RCV005225744]	uncertain significance	2	218892915	218892915	Human	1	name
597852180	CV3869640	single nucleotide variant	NM_025216.3(WNT10A):c.338G>C (p.Arg113Pro)	Odonto-onycho-dermal dysplasia [RCV005212924]	uncertain significance	2	218882385	218882385	Human	1	name
597858661	CV3877822	single nucleotide variant	NM_025216.3(WNT10A):c.319T>A (p.Cys107Ser)	Odonto-onycho-dermal dysplasia [RCV005229131]	uncertain significance	2	218882366	218882366	Human	1	name
597931149	CV3878549	single nucleotide variant	NM_025216.3(WNT10A):c.839C>T (p.Thr280Met)	Odonto-onycho-dermal dysplasia [RCV005224919]	uncertain significance	2	218892856	218892856	Human	1	name
598126584	CV3882033	single nucleotide variant	NM_003394.4(WNT10B):c.718A>G (p.Thr240Ala)	not provided [RCV005233585]	uncertain significance	12	48966547	48966547	Human		name
598235864	CV3893521	single nucleotide variant	NM_025216.3(WNT10A):c.823A>G (p.Thr275Ala)	not provided [RCV005256254]	uncertain significance	2	218892840	218892840	Human		name
598275507	CV3937152	single nucleotide variant	NM_025216.3(WNT10A):c.523C>T (p.His175Tyr)	Inborn genetic diseases [RCV005304641]	uncertain significance	2	218890130	218890130	Human	1	name
598275509	CV3937154	single nucleotide variant	NM_025216.3(WNT10A):c.370A>G (p.Ser124Gly)	Inborn genetic diseases [RCV005304643]	uncertain significance	2	218882417	218882417	Human	1	name
598275511	CV3937156	single nucleotide variant	NM_025216.3(WNT10A):c.949G>C (p.Ala317Pro)	Inborn genetic diseases [RCV005304645]	uncertain significance	2	218892966	218892966	Human	1	name
598236056	CV3937157	single nucleotide variant	NM_003394.4(WNT10B):c.467G>A (p.Arg156Gln)	Inborn genetic diseases [RCV005295953]	uncertain significance	12	48968190	48968190	Human	1	name
598236066	CV3937159	single nucleotide variant	NM_003394.4(WNT10B):c.899G>A (p.Arg300His)	Inborn genetic diseases [RCV005295955]	uncertain significance	12	48966366	48966366	Human	1	name
598236087	CV3937163	single nucleotide variant	NM_004626.3(WNT11):c.1043T>C (p.Val348Ala)	not specified [RCV005295959]	uncertain significance	11	76187087	76187087	Human		name
8568434	CV39524	single nucleotide variant	NM_025216.3(WNT10A):c.649G>A (p.Asp217Asn)	Odonto-onycho-dermal dysplasia [RCV000322248]\|Odonto-onycho-dermal dysplasia [RCV002513192]\|SchC6pf-Schulz-Passarge syndrome [RCV000271824]\|Tooth agenesis, selective, 4 [RCV000023530]\|not provided [RCV000059804]\|not specified [RCV002247385]	pathogenic\|likely benign\|uncertain significance\|not provided	2	218890256	218890256	Human	3	name
12892767	CV404757	single nucleotide variant	NM_025216.3(WNT10A):c.616C>T (p.Gln206Ter)	Odonto-onycho-dermal dysplasia [RCV000477883]	likely pathogenic	2	218890223	218890223	Human	1	name
13473767	CV450631	single nucleotide variant	NM_025216.3(WNT10A):c.433G>A (p.Val145Met)	Odonto-onycho-dermal dysplasia [RCV000525525]\|Odonto-onycho-dermal dysplasia [RCV002289759]\|Odonto-onycho-dermal dysplasia [RCV005018927]\|SchC6pf-Schulz-Passarge syndrome [RCV001275114]	pathogenic\|likely pathogenic\|uncertain significance	2	218890040	218890040	Human	3	name
13481568	CV450717	single nucleotide variant	NM_025216.3(WNT10A):c.382C>T (p.Arg128Ter)	Odonto-onycho-dermal dysplasia [RCV000551493]\|Odonto-onycho-dermal dysplasia [RCV000763071]\|SchC6pf-Schulz-Passarge syndrome [RCV001829582]\|not provided [RCV000760328]	pathogenic\|likely pathogenic	2	218889989	218889989	Human	3	name
13518753	CV486079	single nucleotide variant	NM_003394.4(WNT10B):c.995G>A (p.Arg332Gln)	Split hand-foot malformation 6 [RCV003227802]\|not provided [RCV000585078]	uncertain significance	12	48966270	48966270	Human	1	name
13532274	CV511396	single nucleotide variant	NM_025216.3(WNT10A):c.725T>G (p.Met242Arg)	Inborn genetic diseases [RCV000624049]	likely pathogenic\|uncertain significance	2	218890332	218890332	Human	1	name
13607901	CV517834	single nucleotide variant	NM_025216.3(WNT10A):c.310C>T (p.Arg104Cys)	Odonto-onycho-dermal dysplasia [RCV000639735]\|Odonto-onycho-dermal dysplasia [RCV003329168]\|Odonto-onycho-dermal dysplasia [RCV005019061]\|not provided [RCV001756063]	pathogenic\|likely pathogenic\|uncertain significance	2	218882357	218882357	Human	1	name
13607898	CV517936	single nucleotide variant	NM_025216.3(WNT10A):c.831G>T (p.Trp277Cys)	Odonto-onycho-dermal dysplasia [RCV000639738]\|SchC6pf-Schulz-Passarge syndrome [RCV001829792]	uncertain significance	2	218892848	218892848	Human	3	name
13607899	CV517938	single nucleotide variant	NM_025216.3(WNT10A):c.910A>C (p.Asn304His)	Odonto-onycho-dermal dysplasia [RCV000639737]\|Odonto-onycho-dermal dysplasia [RCV005027754]\|SchC6pf-Schulz-Passarge syndrome [RCV001835029]	pathogenic\|likely pathogenic\|uncertain significance	2	218892927	218892927	Human	3	name
13790555	CV550123	single nucleotide variant	NM_025216.3(WNT10A):c.826T>A (p.Cys276Ser)	Odonto-onycho-dermal dysplasia [RCV000677102]	pathogenic	2	218892843	218892843	Human	1	name
13816674	CV559117	single nucleotide variant	NM_025216.3(WNT10A):c.695G>A (p.Arg232Gln)	Odonto-onycho-dermal dysplasia [RCV000706483]\|SchC6pf-Schulz-Passarge syndrome [RCV001825399]	uncertain significance	2	218890302	218890302	Human	3	name
13814522	CV559119	single nucleotide variant	NM_025216.3(WNT10A):c.959C>G (p.Pro320Arg)	Odonto-onycho-dermal dysplasia [RCV000705093]	uncertain significance	2	218892976	218892976	Human	1	name
13821793	CV560936	single nucleotide variant	NM_025216.3(WNT10A):c.403G>A (p.Ala135Thr)	Odonto-onycho-dermal dysplasia [RCV000696391]\|Odonto-onycho-dermal dysplasia [RCV005027867]\|SchC6pf-Schulz-Passarge syndrome [RCV001830529]	likely pathogenic\|uncertain significance	2	218890010	218890010	Human	3	name
14696549	CV622269	single nucleotide variant	NM_025216.3(WNT10A):c.311G>A (p.Arg104His)	Odonto-onycho-dermal dysplasia [RCV001047681]\|Odonto-onycho-dermal dysplasia [RCV005021173]\|Tooth agenesis, selective, 4 [RCV000782362]\|not provided [RCV001546388]	pathogenic\|likely pathogenic\|conflicting interpretations of pathogenicity\|uncertain significance	2	218882358	218882358	Human	2	name
14695947	CV622516	single nucleotide variant	NM_003394.4(WNT10B):c.949T>A (p.Phe317Ile)	Split hand-foot malformation 6 [RCV000785183]	likely pathogenic	12	48966316	48966316	Human	1	name
14695946	CV622519	single nucleotide variant	NM_003394.4(WNT10B):c.746G>T (p.Cys249Phe)	Split hand-foot malformation 6 [RCV000785181]	likely pathogenic	12	48966519	48966519	Human	1	name
14730856	CV629468	single nucleotide variant	NM_025216.3(WNT10A):c.554G>A (p.Gly185Asp)	Odonto-onycho-dermal dysplasia [RCV000801132]	uncertain significance	2	218890161	218890161	Human	1	name
15150327	CV697327	single nucleotide variant	NM_025216.3(WNT10A):c.874A>G (p.Ser292Gly)	Odonto-onycho-dermal dysplasia [RCV000945473]\|SchC6pf-Schulz-Passarge syndrome [RCV001275116]	likely benign	2	218892891	218892891	Human	3	name
8625301	CV80420	single nucleotide variant	NM_025216.2(WNT10A):c.431C>T (p.Ala144Val)	Malignant melanoma [RCV000060497]	not provided	2	218890038	218890038	Human		name
8627293	CV82437	single nucleotide variant	NM_003394.3(WNT10B):c.698G>A (p.Arg233Lys)	Malignant melanoma [RCV000062516]	not provided	12	48967959	48967959	Human		name
26891873	CV825746	single nucleotide variant	NM_025216.3(WNT10A):c.791G>T (p.Cys264Phe)	Odonto-onycho-dermal dysplasia [RCV001068439]	uncertain significance	2	218892808	218892808	Human	1	name
26886192	CV825747	single nucleotide variant	NM_025216.3(WNT10A):c.814C>T (p.Gln272Ter)	Odonto-onycho-dermal dysplasia [RCV001044035]\|Odonto-onycho-dermal dysplasia [RCV002497378]\|Tooth agenesis, selective, 4 [RCV002290566]\|not provided [RCV001784592]	pathogenic\|likely pathogenic	2	218892831	218892831	Human	2	name
28890025	CV883767	single nucleotide variant	NM_025216.3(WNT10A):c.526C>T (p.Arg176Cys)	Odonto-onycho-dermal dysplasia [RCV001138902]\|Odonto-onycho-dermal dysplasia [RCV005209534]\|SchC6pf-Schulz-Passarge syndrome [RCV001138904]\|Tooth agenesis, selective, 4 [RCV001138903]	uncertain significance	2	218890133	218890133	Human	3	name
28882924	CV883768	single nucleotide variant	NM_025216.3(WNT10A):c.653T>G (p.Met218Arg)	Odonto-onycho-dermal dysplasia [RCV001143338]\|SchC6pf-Schulz-Passarge syndrome [RCV001136765]\|Tooth agenesis, selective, 4 [RCV001136766]	uncertain significance	2	218890260	218890260	Human	3	name
28882928	CV883769	single nucleotide variant	NM_025216.3(WNT10A):c.664G>A (p.Glu222Lys)	Odonto-onycho-dermal dysplasia [RCV001136768]\|SchC6pf-Schulz-Passarge syndrome [RCV001136767]\|Tooth agenesis, selective, 4 [RCV001136769]	uncertain significance	2	218890271	218890271	Human	3	name
28882936	CV883770	single nucleotide variant	NM_025216.3(WNT10A):c.668G>A (p.Arg223His)	Odonto-onycho-dermal dysplasia [RCV001136772]\|Odonto-onycho-dermal dysplasia [RCV002491408]\|Odonto-onycho-dermal dysplasia [RCV003106128]\|SchC6pf-Schulz-Passarge syndrome [RCV001136770]\|Tooth agenesis, selective, 4 [RCV001136771]	uncertain significance	2	218890275	218890275	Human	3	name
28890340	CV883771	single nucleotide variant	NM_025216.3(WNT10A):c.694C>T (p.Arg232Trp)	Odonto-onycho-dermal dysplasia [RCV001139006]\|SchC6pf-Schulz-Passarge syndrome [RCV001139004]\|Tooth agenesis, selective, 4 [RCV001139005]	uncertain significance	2	218890301	218890301	Human	3	name
28890346	CV883772	single nucleotide variant	NM_025216.3(WNT10A):c.697G>A (p.Glu233Lys)	Odonto-onycho-dermal dysplasia [RCV001139007]\|Odonto-onycho-dermal dysplasia [RCV001856783]\|SchC6pf-Schulz-Passarge syndrome [RCV001141617]\|Tooth agenesis, selective, 4 [RCV001139008]	benign\|uncertain significance	2	218890304	218890304	Human	3	name
38461028	CV931154	single nucleotide variant	NM_025216.3(WNT10A):c.632G>A (p.Trp211Ter)	Odonto-onycho-dermal dysplasia [RCV001211943]	pathogenic	2	218890239	218890239	Human	1	name
38475605	CV931155	single nucleotide variant	NM_025216.3(WNT10A):c.664G>T (p.Glu222Ter)	Inborn genetic diseases [RCV004963184]\|Odonto-onycho-dermal dysplasia [RCV001204324]	pathogenic	2	218890271	218890271	Human	2	name
38457566	CV942612	single nucleotide variant	NM_025216.3(WNT10A):c.830G>A (p.Trp277Ter)	Odonto-onycho-dermal dysplasia [RCV001228664]	pathogenic	2	218892847	218892847	Human	1	name
38471573	CV952940	single nucleotide variant	NM_025216.3(WNT10A):c.427C>T (p.His143Tyr)	Odonto-onycho-dermal dysplasia [RCV001248684]\|SchC6pf-Schulz-Passarge syndrome [RCV001830048]\|not specified [RCV003323833]	uncertain significance	2	218890034	218890034	Human	3	name
38492153	CV952941	single nucleotide variant	NM_025216.3(WNT10A):c.796G>A (p.Gly266Ser)	Odonto-onycho-dermal dysplasia [RCV001239932]\|SchC6pf-Schulz-Passarge syndrome [RCV001834106]	uncertain significance	2	218892813	218892813	Human	3	name
38499633	CV952942	single nucleotide variant	NM_025216.3(WNT10A):c.914G>A (p.Arg305His)	Inborn genetic diseases [RCV002568604]\|Odonto-onycho-dermal dysplasia [RCV001244885]\|SchC6pf-Schulz-Passarge syndrome [RCV001835217]	uncertain significance	2	218892931	218892931	Human	4	name
40887261	CV973279	single nucleotide variant	NM_025216.3(WNT10A):c.958C>T (p.Pro320Ser)	Inborn genetic diseases [RCV001266754]\|SchC6pf-Schulz-Passarge syndrome [RCV001835357]	uncertain significance	2	218892975	218892975	Human	2	name
150554140	CV1296530	single nucleotide variant	NM_003394.4(WNT10B):c.1087C>T (p.Arg363Cys)	not provided [RCV001770767]	uncertain significance	12	48966178	48966178	Human		name
151725567	CV1356667	single nucleotide variant	NM_025216.3(WNT10A):c.1028C>T (p.Pro343Leu)	Odonto-onycho-dermal dysplasia [RCV001910291]	likely pathogenic\|uncertain significance	2	218893045	218893045	Human	1	name
151797539	CV1470527	single nucleotide variant	NM_003394.4(WNT10B):c.1157A>G (p.Asn386Ser)	not provided [RCV001898757]	uncertain significance	12	48966108	48966108	Human		name
153000876	CV1683900	single nucleotide variant	NM_025216.3(WNT10A):c.1042C>T (p.Arg348Cys)	Abnormality of the dentition [RCV002254494]	uncertain significance	2	218893059	218893059	Human	1	name
156390698	CV1872692	single nucleotide variant	NM_025216.3(WNT10A):c.1018G>T (p.Glu340Ter)	Odonto-onycho-dermal dysplasia [RCV003051281]	pathogenic	2	218893035	218893035	Human	1	name
156444506	CV1938366	single nucleotide variant	NM_025216.3(WNT10A):c.1204G>A (p.Val402Met)	Odonto-onycho-dermal dysplasia [RCV003115430]	uncertain significance	2	218893221	218893221	Human	1	name
8558102	CV19503	single nucleotide variant	NM_025216.3(WNT10A):c.1128C>A (p.Cys376Ter)	Odonto-onycho-dermal dysplasia [RCV000004719]\|Odonto-onycho-dermal dysplasia [RCV003764526]	pathogenic	2	218893145	218893145	Human	1	name
156107381	CV1992370	single nucleotide variant	NM_003394.4(WNT10B):c.1063G>A (p.Val355Met)	not provided [RCV002622440]	uncertain significance	12	48966202	48966202	Human		name
156192457	CV2099051	single nucleotide variant	NM_025216.3(WNT10A):c.1154G>A (p.Arg385His)	Odonto-onycho-dermal dysplasia [RCV002917493]	uncertain significance	2	218893171	218893171	Human	1	name
156334203	CV2112977	single nucleotide variant	NM_025216.3(WNT10A):c.1247G>C (p.Cys416Ser)	Odonto-onycho-dermal dysplasia [RCV002938535]	uncertain significance	2	218893264	218893264	Human	1	name
156197554	CV2157344	single nucleotide variant	NM_025216.3(WNT10A):c.1223G>A (p.Arg408His)	Odonto-onycho-dermal dysplasia [RCV003006212]	uncertain significance	2	218893240	218893240	Human	1	name
156146662	CV2212775	single nucleotide variant	NM_025216.3(WNT10A):c.1004A>C (p.Asp335Ala)	Inborn genetic diseases [RCV002697385]	uncertain significance	2	218893021	218893021	Human	1	name
243053377	CV2416309	single nucleotide variant	NM_003394.4(WNT10B):c.1069C>T (p.Arg357Trp)	not provided [RCV003149370]	uncertain significance	12	48966196	48966196	Human		name
329359101	CV2435290	single nucleotide variant	NM_003394.4(WNT10B):c.1070G>A (p.Arg357Gln)	Inborn genetic diseases [RCV003179234]	uncertain significance	12	48966195	48966195	Human	1	name
329848060	CV2667679	single nucleotide variant	NM_003394.4(WNT10B):c.1127G>A (p.Cys376Tyr)	not provided [RCV003229246]	uncertain significance	12	48966138	48966138	Human		name
401734084	CV2688399	single nucleotide variant	NM_025216.3(WNT10A):c.1237G>A (p.Val413Ile)	Inborn genetic diseases [RCV003290666]	uncertain significance	2	218893254	218893254	Human	1	name
401799316	CV2741879	single nucleotide variant	NM_025216.3(WNT10A):c.1066G>A (p.Gly356Ser)	Odonto-onycho-dermal dysplasia [RCV003323311]	likely pathogenic	2	218893083	218893083	Human	1	name
401796953	CV2741880	single nucleotide variant	NM_025216.3(WNT10A):c.1070C>T (p.Thr357Ile)	Odonto-onycho-dermal dysplasia [RCV003777343]\|Tooth agenesis, selective, 4 [RCV003323312]	pathogenic\|likely pathogenic	2	218893087	218893087	Human	2	name
401797098	CV2741926	single nucleotide variant	NM_025216.3(WNT10A):c.1124T>C (p.Met375Thr)	Tooth agenesis, selective, 4 [RCV003324105]	likely pathogenic\|uncertain significance\|low penetrance	2	218893141	218893141	Human	1	name
401830069	CV2747776	single nucleotide variant	NM_025216.3(WNT10A):c.1127G>T (p.Cys376Phe)	Tooth agenesis, selective, 4 [RCV003329221]	uncertain significance	2	218893144	218893144	Human	1	name
401916100	CV2829389	single nucleotide variant	NM_025216.3(WNT10A):c.1151T>A (p.Leu384Gln)	not provided [RCV003443238]	uncertain significance	2	218893168	218893168	Human		name
11578738	CV284769	single nucleotide variant	NM_025216.3(WNT10A):c.1003G>A (p.Asp335Asn)	Odonto-onycho-dermal dysplasia [RCV000347757]\|Odonto-onycho-dermal dysplasia [RCV000876005]\|Odonto-onycho-dermal dysplasia [RCV002502293]\|SchC6pf-Schulz-Passarge syndrome [RCV000397812]\|Tooth agenesis, selective, 4 [RCV000288085]	benign\|likely benign	2	218893020	218893020	Human	3	name
11582510	CV285423	single nucleotide variant	NM_025216.3(WNT10A):c.1049C>T (p.Pro350Leu)	Odonto-onycho-dermal dysplasia [RCV000355122]\|SchC6pf-Schulz-Passarge syndrome [RCV000304817]\|Tooth agenesis, selective, 4 [RCV000260245]\|not provided [RCV003114495]	likely benign\|uncertain significance	2	218893066	218893066	Human	3	name
11584384	CV287892	single nucleotide variant	NM_025216.3(WNT10A):c.1061C>T (p.Ser354Leu)	Odonto-onycho-dermal dysplasia [RCV000320197]\|SchC6pf-Schulz-Passarge syndrome [RCV000356293]\|Tooth agenesis, selective, 4 [RCV000273350]	uncertain significance	2	218893078	218893078	Human	3	name
11586534	CV287901	single nucleotide variant	NM_025216.3(WNT10A):c.1087A>C (p.Asn363His)	Odonto-onycho-dermal dysplasia [RCV000387692]\|Odonto-onycho-dermal dysplasia [RCV001082463]\|Odonto-onycho-dermal dysplasia [RCV005355656]\|SchC6pf-Schulz-Passarge syndrome [RCV000333165]\|Tooth agenesis [RCV000845114]\|Tooth agenesis, selective, 4 [RCV000288484]\|not provided [RCV000414053]\|not specifie ... (more) d [RCV002248620]	pathogenic\|likely pathogenic\|benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	218893104	218893104	Human	5	name
402525200	CV3086749	single nucleotide variant	NM_025216.3(WNT10A):c.1036T>C (p.Cys346Arg)	Odonto-onycho-dermal dysplasia [RCV003781366]	uncertain significance	2	218893053	218893053	Human	1	name
402515833	CV3089802	single nucleotide variant	NM_025216.3(WNT10A):c.1040A>C (p.Glu347Ala)	Odonto-onycho-dermal dysplasia [RCV003780677]	uncertain significance	2	218893057	218893057	Human	1	name
405074156	CV3103999	duplication	NM_025216.3(WNT10A):c.99_105dup (p.Met36fs)	Odonto-onycho-dermal dysplasia [RCV003799669]	pathogenic	2	218881092	218881093	Human	1	name
405110071	CV3110557	single nucleotide variant	NM_025216.3(WNT10A):c.1127G>C (p.Cys376Ser)	Odonto-onycho-dermal dysplasia [RCV003813460]	uncertain significance	2	218893144	218893144	Human	1	name
405812089	CV3352907	single nucleotide variant	NM_025216.3(WNT10A):c.1052G>T (p.Arg351Leu)	Inborn genetic diseases [RCV004483107]	uncertain significance	2	218893069	218893069	Human	1	name
12849406	CV366372	single nucleotide variant	NM_025216.3(WNT10A):c.1168G>T (p.Glu390Ter)	Odonto-onycho-dermal dysplasia [RCV001232141]\|Odonto-onycho-dermal dysplasia [RCV004786688]\|not provided [RCV000429425]	pathogenic\|likely pathogenic	2	218893185	218893185	Human	1	name
597834135	CV3864223	single nucleotide variant	NM_025216.3(WNT10A):c.1181G>A (p.Cys394Tyr)	Odonto-onycho-dermal dysplasia [RCV005209859]	uncertain significance	2	218893198	218893198	Human	1	name
597834696	CV3864318	single nucleotide variant	NM_025216.3(WNT10A):c.1138G>A (p.Gly380Ser)	Odonto-onycho-dermal dysplasia [RCV005209954]	uncertain significance	2	218893155	218893155	Human	1	name
598275508	CV3937153	single nucleotide variant	NM_025216.3(WNT10A):c.1098C>A (p.Ser366Arg)	Inborn genetic diseases [RCV005304642]	uncertain significance	2	218893115	218893115	Human	1	name
598275510	CV3937155	single nucleotide variant	NM_025216.3(WNT10A):c.1211G>T (p.Cys404Phe)	Inborn genetic diseases [RCV005304644]	uncertain significance	2	218893228	218893228	Human	1	name
12907283	CV414869	single nucleotide variant	NM_025216.3(WNT10A):c.1247G>A (p.Cys416Tyr)	Odonto-onycho-dermal dysplasia [RCV005355978]\|not provided [RCV000490252]	likely pathogenic	2	218893264	218893264	Human	1	name
13212367	CV425469	single nucleotide variant	NM_025216.3(WNT10A):c.1084T>C (p.Cys362Arg)	Odonto-onycho-dermal dysplasia [RCV001379319]\|not provided [RCV000498719]	pathogenic\|likely pathogenic	2	218893101	218893101	Human	1	name
13478520	CV445016	single nucleotide variant	NM_003394.4(WNT10B):c.1087C>G (p.Arg363Gly)	not provided [RCV000520692]	uncertain significance	12	48966178	48966178	Human		name
13495976	CV450635	single nucleotide variant	NM_025216.3(WNT10A):c.1212C>G (p.Cys404Trp)	Odonto-onycho-dermal dysplasia [RCV000537520]	uncertain significance	2	218893229	218893229	Human	1	name
13494847	CV450724	single nucleotide variant	NM_025216.3(WNT10A):c.1034T>C (p.Phe345Ser)	Odonto-onycho-dermal dysplasia [RCV000559209]\|not provided [RCV004760569]	likely pathogenic\|uncertain significance	2	218893051	218893051	Human	1	name
13790551	CV550122	single nucleotide variant	NM_025216.3(WNT10A):c.1176C>A (p.Cys392Ter)	Odonto-onycho-dermal dysplasia [RCV000677099]	pathogenic	2	218893193	218893193	Human	1	name
14713475	CV629472	single nucleotide variant	NM_025216.3(WNT10A):c.1079G>T (p.Arg360Leu)	Odonto-onycho-dermal dysplasia [RCV000810581]\|not specified [RCV003317379]	pathogenic\|uncertain significance	2	218893096	218893096	Human	1	name
14718553	CV629473	single nucleotide variant	NM_025216.3(WNT10A):c.1085G>T (p.Cys362Phe)	Odonto-onycho-dermal dysplasia [RCV000795841]	uncertain significance	2	218893102	218893102	Human	1	name
21075086	CV798498	single nucleotide variant	NM_025216.3(WNT10A):c.1199G>A (p.Cys400Tyr)	Odonto-onycho-dermal dysplasia [RCV000995914]	pathogenic	2	218893216	218893216	Human	1	name
26894512	CV825749	single nucleotide variant	NM_025216.3(WNT10A):c.1079G>C (p.Arg360Pro)	Odonto-onycho-dermal dysplasia [RCV001069353]	likely pathogenic\|uncertain significance	2	218893096	218893096	Human	1	name
28890650	CV883774	single nucleotide variant	NM_025216.3(WNT10A):c.1035C>A (p.Phe345Leu)	Odonto-onycho-dermal dysplasia [RCV001139115]\|SchC6pf-Schulz-Passarge syndrome [RCV001141724]\|Tooth agenesis, selective, 4 [RCV001141723]	uncertain significance	2	218893052	218893052	Human	3	name
38489792	CV922578	single nucleotide variant	NM_025216.3(WNT10A):c.1114T>G (p.Cys372Gly)	Odonto-onycho-dermal dysplasia [RCV001221860]\|not provided [RCV002275316]	pathogenic\|uncertain significance	2	218893131	218893131	Human	1	name
38483165	CV922579	single nucleotide variant	NM_025216.3(WNT10A):c.1124T>G (p.Met375Arg)	Odonto-onycho-dermal dysplasia [RCV001218811]\|SchC6pf-Schulz-Passarge syndrome [RCV001828740]	uncertain significance	2	218893141	218893141	Human	3	name
38485224	CV931156	single nucleotide variant	NM_025216.3(WNT10A):c.1199G>C (p.Cys400Ser)	Odonto-onycho-dermal dysplasia [RCV001208383]	uncertain significance	2	218893216	218893216	Human	1	name
40904349	CV977687	single nucleotide variant	NM_025216.3(WNT10A):c.1162C>T (p.Arg388Cys)	SchC6pf-Schulz-Passarge syndrome [RCV001277358]\|not provided [RCV004692387]	uncertain significance	2	218893179	218893179	Human	1	name
151348364	CV1324008	deletion	NM_003394.4(WNT10B):c.117_136del (p.Glu39fs)	Split hand-foot malformation 6 [RCV001807920]	pathogenic	12	48970290	48970309	Human	1	name
405867938	CV3401329	indel	NM_025216.3(WNT10A):c.62delinsGA (p.Ala21fs)	Odonto-onycho-dermal dysplasia [RCV004577640]	pathogenic	2	218881057	218881057	Human		name
596932199	CV3533909	duplication	NM_004626.3(WNT11):c.677_678dup (p.Leu227fs)	not provided [RCV004781974]	uncertain significance	11	76191775	76191776	Human		name
127254871	CV1059192	duplication	NM_025216.3(WNT10A):c.495_502dup (p.Glu168fs)	Odonto-onycho-dermal dysplasia [RCV001386230]	pathogenic	2	218890096	218890097	Human	1	name
127268306	CV1059195	deletion	NM_025216.3(WNT10A):c.847_851del (p.Phe283fs)	Odonto-onycho-dermal dysplasia [RCV001389202]	pathogenic	2	218892863	218892867	Human	1	name
151772999	CV1502180	deletion	NM_025216.3(WNT10A):c.532_536del (p.Gln178fs)	Odonto-onycho-dermal dysplasia [RCV001929713]	pathogenic	2	218890139	218890143	Human	1	name
153304786	CV1690753	deletion	NM_003394.4(WNT10B):c.499_500del (p.Leu167fs)	Split hand-foot malformation 6 [RCV002269797]	pathogenic	12	48968157	48968158	Human	1	name
156079758	CV2138120	microsatellite	NM_025216.3(WNT10A):c.983_984del (p.Arg328fs)	Odonto-onycho-dermal dysplasia [RCV002979218]	pathogenic	2	218892997	218892998	Human		name
156254222	CV2154102	deletion	NM_003394.4(WNT10B):c.884_896del (p.Phe295fs)	not provided [RCV003008548]	pathogenic	12	48966369	48966381	Human		name
156141037	CV2191850	duplication	NM_025216.3(WNT10A):c.982_986dup (p.Arg330fs)	Odonto-onycho-dermal dysplasia [RCV003056185]	pathogenic	2	218892994	218892995	Human	1	name
405003524	CV3102202	duplication	NM_025216.3(WNT10A):c.981_993dup (p.Ser332fs)	Odonto-onycho-dermal dysplasia [RCV003804248]	pathogenic	2	218892991	218892992	Human	1	name
597842283	CV3865029	deletion	NM_025216.3(WNT10A):c.799_800del (p.Thr267fs)	Odonto-onycho-dermal dysplasia [RCV005211477]	pathogenic	2	218892815	218892816	Human	1	name
8568214	CV39193	duplication	NM_003394.4(WNT10B):c.458_461dup (p.Asp155fs)	Split hand-foot malformation 6 [RCV000023161]	pathogenic	12	48968195	48968196	Human	1	name
13790554	CV550120	deletion	NM_025216.3(WNT10A):c.898_899del (p.Ile300fs)	Odonto-onycho-dermal dysplasia [RCV000677101]	pathogenic	2	218892915	218892916	Human	1	name
13807390	CV557933	deletion	NM_025216.3(WNT10A):c.903_906del (p.Pro302fs)	Odonto-onycho-dermal dysplasia [RCV000686716]	pathogenic\|uncertain significance	2	218892917	218892920	Human	1	name
14353688	CV590508	microsatellite	NM_003394.4(WNT10B):c.689ACA[2] (p.Asn232del)	Split hand-foot malformation 6 [RCV000735854]\|not provided [RCV004800566]	pathogenic\|likely pathogenic	12	48967960	48967962	Human		name
26893463	CV825748	deletion	NM_025216.3(WNT10A):c.909_916del (p.His303fs)	Odonto-onycho-dermal dysplasia [RCV001047325]	pathogenic	2	218892921	218892928	Human	1	name
127247899	CV1059198	duplication	NM_025216.3(WNT10A):c.990_1003dup (p.Asp335fs)	Odonto-onycho-dermal dysplasia [RCV001384812]\|not provided [RCV003132491]	pathogenic\|likely pathogenic	2	218893004	218893005	Human	1	name
13811446	CV560938	duplication	NM_025216.3(WNT10A):c.987_989dup (p.Arg330dup)	Odonto-onycho-dermal dysplasia [RCV000703069]\|SchC6pf-Schulz-Passarge syndrome [RCV001825386]	uncertain significance	2	218893001	218893002	Human	3	name
40903639	CV917746	duplication	NM_025216.3(WNT10A):c.916_918dup (p.Asn306dup)	Tooth agenesis, selective, 4 [RCV001269382]	uncertain significance	2	218892931	218892932	Human	1	name
597635117	CV3706111	deletion	NM_025216.3(WNT10A):c.1226_1230del (p.Ile409fs)	Odonto-onycho-dermal dysplasia [RCV005024086]	pathogenic	2	218893243	218893247	Human	1	name

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