Lrrc3 Variant Search Result - Rat Genome Database

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886 records found for search term Lrrc3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598250767	CV3988258	single nucleotide variant	NM_030891.6(LRRC3):c.10G>A (p.Val4Met)	not specified [RCV005366568]	uncertain significance	21	44456654	44456654	Human		name
156313734	CV2196543	single nucleotide variant	NM_030891.6(LRRC3):c.49C>T (p.Arg17Trp)	not specified [RCV004073831]	uncertain significance	21	44456693	44456693	Human		name
401863782	CV2770825	single nucleotide variant	NM_030891.6(LRRC3):c.67C>T (p.Leu23Phe)	not specified [RCV004349857]	uncertain significance	21	44456711	44456711	Human		name
597778498	CV3696777	single nucleotide variant	NM_030891.6(LRRC3):c.44C>G (p.Ser15Cys)	not specified [RCV004930144]	uncertain significance	21	44456688	44456688	Human		name
598272842	CV3988253	single nucleotide variant	NM_030891.6(LRRC3):c.29C>G (p.Ser10Trp)	not specified [RCV005350577]	uncertain significance	21	44456673	44456673	Human		name
598231516	CV3988261	single nucleotide variant	NM_030891.6(LRRC3):c.31C>G (p.Leu11Val)	not specified [RCV005362878]	uncertain significance	21	44456675	44456675	Human		name
156033797	CV2211623	single nucleotide variant	NM_030891.6(LRRC3):c.188C>T (p.Pro63Leu)	not specified [RCV004084517]	uncertain significance	21	44456832	44456832	Human		name
156379508	CV2214829	single nucleotide variant	NM_030891.6(LRRC3):c.178G>A (p.Glu60Lys)	not specified [RCV004090623]	likely benign	21	44456822	44456822	Human		name
155949854	CV2242785	single nucleotide variant	NM_030891.6(LRRC3):c.130G>A (p.Gly44Arg)	not specified [RCV004107385]	uncertain significance	21	44456774	44456774	Human		name
156149439	CV2292967	single nucleotide variant	NM_030891.6(LRRC3):c.112C>G (p.Arg38Gly)	not specified [RCV004148452]	uncertain significance	21	44456756	44456756	Human		name
156262521	CV2319793	single nucleotide variant	NM_030891.6(LRRC3):c.134C>T (p.Ala45Val)	not specified [RCV004187321]	uncertain significance	21	44456778	44456778	Human		name
401874978	CV2756156	single nucleotide variant	NM_030891.6(LRRC3):c.158G>A (p.Arg53Gln)	not specified [RCV004338262]	uncertain significance	21	44456802	44456802	Human		name
405655481	CV3277243	single nucleotide variant	NM_030891.6(LRRC3):c.265C>T (p.Arg89Trp)	not specified [RCV004415396]	uncertain significance	21	44456909	44456909	Human		name
407468113	CV3456421	single nucleotide variant	NM_030891.6(LRRC3):c.184A>G (p.Ile62Val)	not specified [RCV004636159]	uncertain significance	21	44456828	44456828	Human		name
407500686	CV3456424	single nucleotide variant	NM_030891.6(LRRC3):c.136G>T (p.Val46Leu)	not specified [RCV004644672]	uncertain significance	21	44456780	44456780	Human		name
597778493	CV3696775	single nucleotide variant	NM_030891.6(LRRC3):c.124C>A (p.His42Asn)	not specified [RCV004930143]	uncertain significance	21	44456768	44456768	Human		name
597625938	CV3696779	single nucleotide variant	NM_030891.6(LRRC3):c.187C>T (p.Pro63Ser)	not specified [RCV004938467]	uncertain significance	21	44456831	44456831	Human		name
598250760	CV3988254	single nucleotide variant	NM_030891.6(LRRC3):c.266G>A (p.Arg89Gln)	not specified [RCV005366567]	likely benign	21	44456910	44456910	Human		name
598272847	CV3988255	single nucleotide variant	NM_030891.6(LRRC3):c.112C>T (p.Arg38Trp)	not specified [RCV005350578]	uncertain significance	21	44456756	44456756	Human		name
598272858	CV3988257	single nucleotide variant	NM_030891.6(LRRC3):c.221A>G (p.Asn74Ser)	not specified [RCV005350580]	uncertain significance	21	44456865	44456865	Human		name
598272864	CV3988260	single nucleotide variant	NM_030891.6(LRRC3):c.293A>G (p.Asn98Ser)	not specified [RCV005350581]	uncertain significance	21	44456937	44456937	Human		name
156058234	CV2305228	single nucleotide variant	NM_030891.6(LRRC3):c.338G>A (p.Gly113Glu)	not specified [RCV004171158]	uncertain significance	21	44456982	44456982	Human		name
156351759	CV2323831	single nucleotide variant	NM_030891.6(LRRC3):c.700C>T (p.Arg234Trp)	not specified [RCV004176365]	uncertain significance	21	44457344	44457344	Human		name
155980991	CV2336984	single nucleotide variant	NM_030891.6(LRRC3):c.760G>A (p.Gly254Ser)	not specified [RCV004192755]	likely benign	21	44457404	44457404	Human		name
401772720	CV2687790	single nucleotide variant	NM_030891.6(LRRC3):c.518A>C (p.His173Pro)	not specified [RCV004302772]	uncertain significance	21	44457162	44457162	Human		name
401776561	CV2703279	single nucleotide variant	NM_030891.6(LRRC3):c.563C>G (p.Ala188Gly)	not specified [RCV004315639]	uncertain significance	21	44457207	44457207	Human		name
401857754	CV2777749	single nucleotide variant	NM_030891.6(LRRC3):c.422G>A (p.Arg141His)	not specified [RCV004345582]	uncertain significance	21	44457066	44457066	Human		name
401883810	CV2785772	single nucleotide variant	NM_030891.6(LRRC3):c.310G>A (p.Gly104Ser)	not specified [RCV004365021]	uncertain significance	21	44456954	44456954	Human		name
405655484	CV3277244	single nucleotide variant	NM_030891.6(LRRC3):c.307A>T (p.Ile103Phe)	not specified [RCV004415397]	uncertain significance	21	44456951	44456951	Human		name
405655486	CV3277245	single nucleotide variant	NM_030891.6(LRRC3):c.346C>T (p.Arg116Trp)	not specified [RCV004415398]	uncertain significance	21	44456990	44456990	Human		name
405655488	CV3277246	single nucleotide variant	NM_030891.6(LRRC3):c.406C>A (p.Leu136Ile)	not specified [RCV004415399]	uncertain significance	21	44457050	44457050	Human		name
405655489	CV3277247	single nucleotide variant	NM_030891.6(LRRC3):c.658G>A (p.Ala220Thr)	not specified [RCV004415400]	likely benign	21	44457302	44457302	Human		name
407468117	CV3456422	single nucleotide variant	NM_030891.6(LRRC3):c.610G>C (p.Asp204His)	not specified [RCV004636160]	uncertain significance	21	44457254	44457254	Human		name
407500681	CV3456423	single nucleotide variant	NM_030891.6(LRRC3):c.680G>A (p.Arg227His)	not specified [RCV004644671]	uncertain significance	21	44457324	44457324	Human		name
407500690	CV3456425	single nucleotide variant	NM_030891.6(LRRC3):c.763C>T (p.Pro255Ser)	not specified [RCV004644673]	uncertain significance	21	44457407	44457407	Human		name
407500694	CV3456426	single nucleotide variant	NM_030891.6(LRRC3):c.347G>A (p.Arg116Gln)	not specified [RCV004644674]	uncertain significance	21	44456991	44456991	Human		name
597625926	CV3696771	single nucleotide variant	NM_030891.6(LRRC3):c.646G>A (p.Ala216Thr)	not specified [RCV004938463]	uncertain significance	21	44457290	44457290	Human		name
597625929	CV3696772	single nucleotide variant	NM_030891.6(LRRC3):c.613G>A (p.Val205Met)	not specified [RCV004938464]	uncertain significance	21	44457257	44457257	Human		name
597778489	CV3696774	single nucleotide variant	NM_030891.6(LRRC3):c.371G>A (p.Arg124His)	not specified [RCV004930142]	uncertain significance	21	44457015	44457015	Human		name
597625932	CV3696776	single nucleotide variant	NM_030891.6(LRRC3):c.371G>T (p.Arg124Leu)	not specified [RCV004938465]	uncertain significance	21	44457015	44457015	Human		name
597625935	CV3696778	single nucleotide variant	NM_030891.6(LRRC3):c.668T>C (p.Val223Ala)	not specified [RCV004938466]	uncertain significance	21	44457312	44457312	Human		name
598272853	CV3988256	single nucleotide variant	NM_030891.6(LRRC3):c.316G>A (p.Ala106Thr)	not specified [RCV005350579]	uncertain significance	21	44456960	44456960	Human		name
598231510	CV3988259	single nucleotide variant	NM_030891.6(LRRC3):c.730C>T (p.Pro244Ser)	not specified [RCV005362877]	uncertain significance	21	44457374	44457374	Human		name
401906503	CV2808214	single nucleotide variant	NM_199340.5(LRRC37A3):c.-537A>G	not provided [RCV003421425]	likely benign	17	64918791	64918791	Human		name
405866935	CV2842427	single nucleotide variant	NM_199340.5(LRRC37A3):c.-561C>T	EBV-positive nodal T- and NK-cell lymphoma [RCV004557784]	likely benign	17	64918815	64918815	Human		name
152155233	CV1668147	single nucleotide variant	NM_001128922.2(LRRC32):c.84+14C>A	Cleft palate, proliferative retinopathy, and developmental delay [RCV002221979]	likely pathogenic	11	76665857	76665857	Human	1	name
155950838	CV1936059	single nucleotide variant	NM_001128922.2(LRRC32):c.*1626C>T	not provided [RCV002511711]	benign	11	76657978	76657978	Human		name
156372718	CV2194560	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-12G>C	not specified [RCV004081621]	uncertain significance	17	32021381	32021381	Human		name
156348968	CV2376369	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-89C>T	not specified [RCV004220563]	uncertain significance	17	32021304	32021304	Human		name
156147420	CV2377247	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-62C>T	not specified [RCV004232306]	uncertain significance	17	32021331	32021331	Human		name
329367282	CV2456751	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-54C>T	not specified [RCV004270728]	uncertain significance	17	32021339	32021339	Human		name
401751057	CV2715853	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-74A>C	not specified [RCV004328969]	uncertain significance	17	32021319	32021319	Human		name
401868152	CV2767158	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-41C>T	not specified [RCV004347554]	uncertain significance	17	32021352	32021352	Human		name
405655758	CV3277374	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-17C>A	not specified [RCV004415527]	uncertain significance	17	32021376	32021376	Human		name
407459722	CV3496871	single nucleotide variant	NM_001172779.2(LRRC34):c.528+1G>A	Autism [RCV004698686]	uncertain significance	3	169806847	169806847	Human	2	name
597626037	CV3696869	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-96C>T	not specified [RCV004938536]	uncertain significance	17	32021297	32021297	Human		name
598250982	CV3984668	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-92C>T	not specified [RCV005366603]	uncertain significance	17	32021301	32021301	Human		name
598273037	CV3984672	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-45G>T	not specified [RCV005350616]	uncertain significance	17	32021348	32021348	Human		name
156160895	CV2371326	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-146C>T	not specified [RCV004223336]	uncertain significance	17	32021247	32021247	Human		name
401858196	CV2766409	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-216C>G	not specified [RCV004345254]	uncertain significance	17	32021177	32021177	Human		name
401935742	CV2811233	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-281T>C	not provided [RCV003413203]	likely benign	17	32021112	32021112	Human		name
405655748	CV3277368	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-234C>T	not specified [RCV004415521]	uncertain significance	17	32021159	32021159	Human		name
405655769	CV3277381	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-148C>A	not specified [RCV004415534]	uncertain significance	17	32021245	32021245	Human		name
407500848	CV3456485	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-156G>T	not specified [RCV004644720]	uncertain significance	17	32021237	32021237	Human		name
597778553	CV3696881	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-102T>C	not specified [RCV004930160]	uncertain significance	17	32021291	32021291	Human		name
597626064	CV3696882	single nucleotide variant	NM_001321350.2(LRRC37B):c.1-162G>A	not specified [RCV004938544]	uncertain significance	17	32021231	32021231	Human		name
8585085	CV119665	single nucleotide variant	NM_001161575.1(LRRC36):c.125+426T>A	Lung cancer [RCV000100185]	uncertain significance	16	67348017	67348017	Human		name
407455951	CV3415787	duplication	NM_001128922.2(LRRC32):c.84+5_84+6dup	not provided [RCV004598663]	uncertain significance	11	76665864	76665865	Human		name
405281617	CV3216114	single nucleotide variant	NM_001128922.2(LRRC32):c.1553G>A (p.Arg518Gln)	LRRC32-related disorder [RCV003956656]	likely benign	11	76660040	76660040	Human		name , trait , alternate_id
405293257	CV3221370	single nucleotide variant	NM_001128922.2(LRRC32):c.497G>A (p.Arg166His)	LRRC32-related disorder [RCV003966871]	uncertain significance	11	76661096	76661096	Human		name , trait , alternate_id
405293309	CV3221405	single nucleotide variant	NM_001128922.2(LRRC32):c.1337G>A (p.Arg446His)	LRRC32-related disorder [RCV003966895]	uncertain significance	11	76660256	76660256	Human		name , trait , alternate_id
408367792	CV3516761	single nucleotide variant	NM_001128922.2(LRRC32):c.1336C>T (p.Arg446Cys)	LRRC32-related disorder [RCV004759245]	likely benign	11	76660257	76660257	Human		name , trait , alternate_id
598250844	CV3988288	single nucleotide variant	NM_018296.6(LRRC36):c.8A>G (p.Glu3Gly)	not specified [RCV005366581]	uncertain significance	16	67326870	67326870	Human		name
156248592	CV2393986	single nucleotide variant	NM_144620.4(LRRC39):c.22A>C (p.Thr8Pro)	not specified [RCV004236209]	uncertain significance	1	100168495	100168495	Human		name
597626089	CV3693385	single nucleotide variant	NM_144620.4(LRRC39):c.22A>G (p.Thr8Ala)	not specified [RCV004938551]	uncertain significance	1	100168495	100168495	Human		name
597778506	CV3696791	single nucleotide variant	NM_024727.4(LRRC31):c.19A>G (p.Lys7Glu)	not specified [RCV004930146]	uncertain significance	3	169869789	169869789	Human		name
598273070	CV3984684	single nucleotide variant	NM_052953.4(LRRC3B):c.24A>C (p.Leu8Phe)	not specified [RCV005350624]	uncertain significance	3	26709696	26709696	Human		name
598251001	CV3984685	single nucleotide variant	NM_052953.4(LRRC3B):c.25A>C (p.Thr9Pro)	not specified [RCV005366606]	uncertain significance	3	26709697	26709697	Human		name
15197995	CV695916	single nucleotide variant	NM_144620.4(LRRC39):c.244C>T (p.Leu82=)	not provided [RCV000956622]	benign	1	100159391	100159391	Human		name
8625598	CV80722	single nucleotide variant	NM_052953.2(LRRC3B):c.240C>T (p.Pro80=)	Malignant melanoma [RCV000060799]	not provided	3	26709912	26709912	Human		name
156007184	CV2357863	single nucleotide variant	NM_052953.4(LRRC3B):c.28C>G (p.Arg10Gly)	not specified [RCV004205144]	uncertain significance	3	26709700	26709700	Human		name
401735033	CV2706637	single nucleotide variant	NM_018296.6(LRRC36):c.74T>C (p.Leu25Pro)	not specified [RCV004319215]	uncertain significance	16	67341960	67341960	Human		name
401752390	CV2723219	single nucleotide variant	NM_052953.4(LRRC3B):c.56A>G (p.Gln19Arg)	not specified [RCV004329455]	uncertain significance	3	26709728	26709728	Human		name
405655532	CV3277267	single nucleotide variant	NM_024727.4(LRRC31):c.98G>A (p.Arg33Lys)	not specified [RCV004415420]	uncertain significance	3	169869710	169869710	Human		name
405655598	CV3277302	single nucleotide variant	NM_018296.6(LRRC36):c.77T>G (p.Val26Gly)	not specified [RCV004415455]	uncertain significance	16	67341963	67341963	Human		name
407500881	CV3456497	single nucleotide variant	NM_144620.4(LRRC39):c.29C>T (p.Ala10Val)	not specified [RCV004644730]	uncertain significance	1	100168488	100168488	Human		name
597778572	CV3693390	single nucleotide variant	NM_052953.4(LRRC3B):c.41T>C (p.Met14Thr)	not specified [RCV004930164]	uncertain significance	3	26709713	26709713	Human		name
597626121	CV3696817	single nucleotide variant	NM_018296.6(LRRC36):c.41G>A (p.Arg14His)	not specified [RCV004938497]	uncertain significance	16	67326903	67326903	Human		name
598272879	CV3988267	single nucleotide variant	NM_024727.4(LRRC31):c.52A>C (p.Thr18Pro)	not specified [RCV005350584]	uncertain significance	3	169869756	169869756	Human		name
598250836	CV3988285	single nucleotide variant	NM_018296.6(LRRC36):c.56C>T (p.Thr19Met)	not specified [RCV005366579]	uncertain significance	16	67326918	67326918	Human		name
598250917	CV3988311	single nucleotide variant	NM_199340.5(LRRC37A3):c.7T>C (p.Ser3Pro)	not specified [RCV005366592]	likely benign	17	64897251	64897251	Human		name
15189654	CV698018	single nucleotide variant	NM_052953.4(LRRC3B):c.573C>T (p.Asp191=)	not provided [RCV000954244]	benign	3	26710245	26710245	Human		name
8624631	CV79744	single nucleotide variant	NM_144620.3(LRRC39):c.62G>A (p.Arg21Lys)	Malignant melanoma [RCV000059820]	not provided	1	100168455	100168455	Human		name
156297215	CV2297655	single nucleotide variant	NM_052953.4(LRRC3B):c.179G>A (p.Arg60Lys)	not specified [RCV004155342]	uncertain significance	3	26709851	26709851	Human		name
156180956	CV2331497	single nucleotide variant	NM_001105581.3(LRRC30):c.7G>A (p.Ala3Thr)	not specified [RCV004184124]	uncertain significance	18	7231145	7231145	Human		name
156339838	CV2351652	single nucleotide variant	NM_024727.4(LRRC31):c.188G>A (p.Ser63Asn)	not specified [RCV004195365]	uncertain significance	3	169861801	169861801	Human		name
401741871	CV2677456	single nucleotide variant	NM_024727.4(LRRC31):c.179A>T (p.Lys60Met)	not specified [RCV004289525]	uncertain significance	3	169861810	169861810	Human		name
401887001	CV2777052	single nucleotide variant	NM_144620.4(LRRC39):c.187G>A (p.Val63Ile)	not specified [RCV004351845]	uncertain significance	1	100160498	100160498	Human		name
405655512	CV3277258	single nucleotide variant	NM_024727.4(LRRC31):c.268T>G (p.Cys90Gly)	not specified [RCV004415411]	uncertain significance	3	169861721	169861721	Human		name
405655515	CV3277259	single nucleotide variant	NM_024727.4(LRRC31):c.274G>A (p.Asp92Asn)	not specified [RCV004415412]	uncertain significance	3	169861715	169861715	Human		name
405655517	CV3277260	single nucleotide variant	NM_024727.4(LRRC31):c.289G>C (p.Gly97Arg)	not specified [RCV004415413]	likely benign	3	169861700	169861700	Human		name
405655781	CV3277388	single nucleotide variant	NM_144620.4(LRRC39):c.200T>C (p.Ile67Thr)	not specified [RCV004415541]	uncertain significance	1	100160485	100160485	Human		name
405655783	CV3277389	single nucleotide variant	NM_144620.4(LRRC39):c.230C>T (p.Ser77Phe)	not specified [RCV004415542]	uncertain significance	1	100159405	100159405	Human		name
407468142	CV3456449	single nucleotide variant	NM_018296.6(LRRC36):c.242A>G (p.Tyr81Cys)	not specified [RCV004636167]	uncertain significance	16	67346299	67346299	Human		name
597626093	CV3693386	single nucleotide variant	NM_144620.4(LRRC39):c.268C>G (p.Leu90Val)	not specified [RCV004938552]	uncertain significance	1	100159367	100159367	Human		name
597626178	CV3693387	single nucleotide variant	NM_144620.4(LRRC39):c.149C>T (p.Thr50Ile)	not specified [RCV004938553]	uncertain significance	1	100160536	100160536	Human		name
597626185	CV3693389	single nucleotide variant	NM_052953.4(LRRC3B):c.155A>G (p.Asn52Ser)	not specified [RCV004938555]	uncertain significance	3	26709827	26709827	Human		name
156144287	CV2208725	single nucleotide variant	NM_001010847.2(LRRC38):c.13G>C (p.Ala5Pro)	not specified [RCV004084914]	uncertain significance	1	13513581	13513581	Human		name
156247930	CV2215379	single nucleotide variant	NM_144620.4(LRRC39):c.602T>C (p.Leu201Pro)	not specified [RCV004089186]	uncertain significance	1	100156229	100156229	Human		name
156247945	CV2215380	single nucleotide variant	NM_144620.4(LRRC39):c.677C>T (p.Thr226Met)	not specified [RCV004089187]	uncertain significance	1	100155186	100155186	Human		name
156227181	CV2216131	single nucleotide variant	NM_144620.4(LRRC39):c.348C>G (p.Asn116Lys)	not specified [RCV004097134]	uncertain significance	1	100159287	100159287	Human		name
156127488	CV2223811	single nucleotide variant	NM_199340.5(LRRC37A3):c.49C>T (p.Arg17Cys)	not provided [RCV004695399]\|not specified [RCV004093870]	uncertain significance	17	64897209	64897209	Human		name
156232721	CV2227702	single nucleotide variant	NM_144620.4(LRRC39):c.839T>C (p.Leu280Pro)	not specified [RCV004094092]	uncertain significance	1	100152498	100152498	Human		name
156289847	CV2229973	single nucleotide variant	NM_024727.4(LRRC31):c.496T>C (p.Phe166Leu)	not specified [RCV004105506]	likely benign	3	169856864	169856864	Human		name
155921777	CV2240577	single nucleotide variant	NM_144620.4(LRRC39):c.706T>A (p.Cys236Ser)	not specified [RCV004119226]	uncertain significance	1	100155157	100155157	Human		name
155922341	CV2240671	single nucleotide variant	NM_144620.4(LRRC39):c.782C>A (p.Pro261Gln)	not specified [RCV004119303]	uncertain significance	1	100155081	100155081	Human		name
156241471	CV2246110	single nucleotide variant	NM_052953.4(LRRC3B):c.574G>A (p.Ala192Thr)	not specified [RCV004114014]	uncertain significance	3	26710246	26710246	Human		name
156078216	CV2248471	single nucleotide variant	NM_018296.6(LRRC36):c.715G>A (p.Ala239Thr)	not specified [RCV004119603]	uncertain significance	16	67365316	67365316	Human		name
155924694	CV2248843	single nucleotide variant	NM_024727.4(LRRC31):c.301G>A (p.Ala101Thr)	not specified [RCV004115856]	uncertain significance	3	169861688	169861688	Human		name
156306590	CV2252755	single nucleotide variant	NM_024727.4(LRRC31):c.404C>T (p.Thr135Ile)	not specified [RCV004118601]	uncertain significance	3	169860644	169860644	Human		name
156357182	CV2253868	single nucleotide variant	NM_018296.6(LRRC36):c.406C>A (p.Arg136Ser)	not specified [RCV004127554]	uncertain significance	16	67347509	67347509	Human		name
156111200	CV2261714	single nucleotide variant	NM_052953.4(LRRC3B):c.664G>T (p.Val222Leu)	not specified [RCV004126015]	uncertain significance	3	26710336	26710336	Human		name
155966195	CV2261886	single nucleotide variant	NM_199340.5(LRRC37A3):c.57G>C (p.Trp19Cys)	not specified [RCV004127939]	uncertain significance	17	64897201	64897201	Human		name
156151746	CV2268974	single nucleotide variant	NM_052953.4(LRRC3B):c.658T>C (p.Tyr220His)	not specified [RCV004128375]	uncertain significance	3	26710330	26710330	Human		name
156273445	CV2277738	single nucleotide variant	NM_024727.4(LRRC31):c.978C>A (p.Asp326Glu)	not specified [RCV004147178]	uncertain significance	3	169854826	169854826	Human		name
156303942	CV2341338	single nucleotide variant	NM_014834.4(LRRC37A):c.174G>C (p.Glu58Asp)	not specified [RCV004186743]	uncertain significance	17	46295307	46295307	Human		name
155921252	CV2350637	single nucleotide variant	NM_144620.4(LRRC39):c.941G>A (p.Arg314Gln)	not specified [RCV004204977]	likely benign	1	100152396	100152396	Human		name
156015954	CV2360360	single nucleotide variant	NM_144620.4(LRRC39):c.892C>T (p.Arg298Trp)	not specified [RCV004208694]	uncertain significance	1	100152445	100152445	Human		name
329373422	CV2434244	single nucleotide variant	NM_144620.4(LRRC39):c.494T>C (p.Ile165Thr)	not specified [RCV004251920]	uncertain significance	1	100158250	100158250	Human		name
329365035	CV2443995	single nucleotide variant	NM_018296.6(LRRC36):c.770C>T (p.Ser257Leu)	not specified [RCV004258320]	uncertain significance	16	67367032	67367032	Human		name
329397109	CV2456605	single nucleotide variant	NM_018296.6(LRRC36):c.463A>G (p.Asn155Asp)	not specified [RCV004277796]	uncertain significance	16	67347566	67347566	Human		name
401737082	CV2679222	single nucleotide variant	NM_024727.4(LRRC31):c.460C>G (p.Leu154Val)	not specified [RCV004285777]	uncertain significance	3	169860588	169860588	Human		name
401729580	CV2683728	single nucleotide variant	NM_018296.6(LRRC36):c.794C>T (p.Ser265Phe)	not specified [RCV004284470]	uncertain significance	16	67367056	67367056	Human		name
401760080	CV2718710	single nucleotide variant	NM_144620.4(LRRC39):c.512A>C (p.Glu171Ala)	not specified [RCV004328466]	uncertain significance	1	100158232	100158232	Human		name
401893918	CV2774342	single nucleotide variant	NM_024727.4(LRRC31):c.608T>C (p.Ile203Thr)	not specified [RCV004347694]	uncertain significance	3	169856752	169856752	Human		name
401888040	CV2781864	single nucleotide variant	NM_024727.4(LRRC31):c.437T>C (p.Ile146Thr)	not specified [RCV004356810]	uncertain significance	3	169860611	169860611	Human		name
401935846	CV2808213	single nucleotide variant	NM_199340.5(LRRC37A3):c.327C>T (p.Phe109=)	not provided [RCV003413308]	likely benign	17	64896931	64896931	Human		name
401929094	CV2813560	single nucleotide variant	NM_001128922.2(LRRC32):c.144G>A (p.Pro48=)	not provided [RCV003390095]	likely benign	11	76661449	76661449	Human		name
405655519	CV3277261	single nucleotide variant	NM_024727.4(LRRC31):c.340C>T (p.Pro114Ser)	not specified [RCV004415414]	uncertain significance	3	169860708	169860708	Human		name
405655521	CV3277262	single nucleotide variant	NM_024727.4(LRRC31):c.365C>T (p.Ser122Phe)	not specified [RCV004415415]	uncertain significance	3	169860683	169860683	Human		name
405655525	CV3277264	single nucleotide variant	NM_024727.4(LRRC31):c.448G>T (p.Gly150Cys)	not specified [RCV004415417]	uncertain significance	3	169860600	169860600	Human		name
405655528	CV3277265	single nucleotide variant	NM_024727.4(LRRC31):c.624C>G (p.Cys208Trp)	not specified [RCV004415418]	uncertain significance	3	169856736	169856736	Human		name
405655530	CV3277266	single nucleotide variant	NM_024727.4(LRRC31):c.703A>G (p.Ile235Val)	not specified [RCV004415419]	uncertain significance	3	169856456	169856456	Human		name
405655595	CV3277300	single nucleotide variant	NM_018296.6(LRRC36):c.563G>A (p.Ser188Asn)	not specified [RCV004415453]	likely benign	16	67350276	67350276	Human		name
405655596	CV3277301	single nucleotide variant	NM_018296.6(LRRC36):c.598A>C (p.Ile200Leu)	not specified [RCV004415454]	uncertain significance	16	67363610	67363610	Human		name
405655785	CV3277391	single nucleotide variant	NM_144620.4(LRRC39):c.326T>C (p.Ile109Thr)	not specified [RCV004415544]	uncertain significance	1	100159309	100159309	Human		name
405655787	CV3277392	single nucleotide variant	NM_144620.4(LRRC39):c.419A>C (p.Lys140Thr)	not specified [RCV004415545]	uncertain significance	1	100158325	100158325	Human		name
405655789	CV3277393	single nucleotide variant	NM_144620.4(LRRC39):c.510A>T (p.Gln170His)	not specified [RCV004415546]	uncertain significance	1	100158234	100158234	Human		name
405655790	CV3277394	single nucleotide variant	NM_144620.4(LRRC39):c.553A>G (p.Met185Val)	not specified [RCV004415547]	uncertain significance	1	100156278	100156278	Human		name
405655792	CV3277395	single nucleotide variant	NM_144620.4(LRRC39):c.625A>C (p.Asn209His)	not specified [RCV004415548]	uncertain significance	1	100156206	100156206	Human		name
405655793	CV3277396	single nucleotide variant	NM_144620.4(LRRC39):c.695A>G (p.Asn232Ser)	not specified [RCV004415549]	uncertain significance	1	100155168	100155168	Human		name
405655795	CV3277397	single nucleotide variant	NM_144620.4(LRRC39):c.789C>G (p.Cys263Trp)	not specified [RCV004415550]	uncertain significance	1	100155074	100155074	Human		name
405655797	CV3277398	single nucleotide variant	NM_052953.4(LRRC3B):c.642C>A (p.Phe214Leu)	not specified [RCV004415551]	uncertain significance	3	26710314	26710314	Human		name
407468146	CV3456450	single nucleotide variant	NM_018296.6(LRRC36):c.791G>C (p.Arg264Pro)	not specified [RCV004636168]	uncertain significance	16	67367053	67367053	Human		name
407500769	CV3456451	single nucleotide variant	NM_018296.6(LRRC36):c.959A>C (p.His320Pro)	not specified [RCV004644691]	uncertain significance	16	67367221	67367221	Human		name
407481607	CV3456493	single nucleotide variant	NM_144620.4(LRRC39):c.976A>G (p.Thr326Ala)	not specified [RCV004644726]	uncertain significance	1	100149074	100149074	Human		name
407500870	CV3456494	single nucleotide variant	NM_144620.4(LRRC39):c.367C>A (p.Pro123Thr)	not specified [RCV004644727]	uncertain significance	1	100159268	100159268	Human		name
407500875	CV3456495	single nucleotide variant	NM_144620.4(LRRC39):c.879T>A (p.Asp293Glu)	not specified [RCV004644728]	uncertain significance	1	100152458	100152458	Human		name
407500885	CV3456498	single nucleotide variant	NM_144620.4(LRRC39):c.947G>T (p.Arg316Ile)	not specified [RCV004644731]	uncertain significance	1	100152390	100152390	Human		name
597626086	CV3693384	single nucleotide variant	NM_144620.4(LRRC39):c.437A>G (p.Lys146Arg)	not specified [RCV004938550]	uncertain significance	1	100158307	100158307	Human		name
597626181	CV3693388	single nucleotide variant	NM_144620.4(LRRC39):c.410G>A (p.Ser137Asn)	not specified [RCV004938554]	uncertain significance	1	100158334	100158334	Human		name
597625954	CV3696784	single nucleotide variant	NM_024727.4(LRRC31):c.866T>G (p.Leu289Arg)	not specified [RCV004938472]	uncertain significance	3	169854938	169854938	Human		name
597625961	CV3696787	single nucleotide variant	NM_024727.4(LRRC31):c.380T>G (p.Val127Gly)	not specified [RCV004938474]	uncertain significance	3	169860668	169860668	Human		name
597625968	CV3696789	single nucleotide variant	NM_024727.4(LRRC31):c.758C>T (p.Thr253Ile)	not specified [RCV004938476]	uncertain significance	3	169856401	169856401	Human		name
597625971	CV3696790	single nucleotide variant	NM_024727.4(LRRC31):c.772G>C (p.Val258Leu)	not specified [RCV004938477]	uncertain significance	3	169856387	169856387	Human		name
597626128	CV3696815	single nucleotide variant	NM_018296.6(LRRC36):c.407G>A (p.Arg136His)	not specified [RCV004938495]	uncertain significance	16	67347510	67347510	Human		name
597626114	CV3696819	single nucleotide variant	NM_018296.6(LRRC36):c.791G>A (p.Arg264Gln)	not specified [RCV004938499]	uncertain significance	16	67367053	67367053	Human		name
597778522	CV3696820	single nucleotide variant	NM_018296.6(LRRC36):c.307G>A (p.Asp103Asn)	not specified [RCV004930150]	uncertain significance	16	67346364	67346364	Human		name
12896757	CV390345	single nucleotide variant	NM_014834.4(LRRC37A):c.2211A>G (p.Pro737=)	not provided [RCV004711107]\|not specified [RCV000455783]	benign	17	46297344	46297344	Human		name
598250996	CV3984683	single nucleotide variant	NM_052953.4(LRRC3B):c.644C>T (p.Thr215Ile)	not specified [RCV005366605]	uncertain significance	3	26710316	26710316	Human		name
598251008	CV3984686	single nucleotide variant	NM_052953.4(LRRC3B):c.752A>G (p.Glu251Gly)	not specified [RCV005366607]	uncertain significance	3	26710424	26710424	Human		name
598222302	CV3984687	single nucleotide variant	NM_052953.4(LRRC3B):c.327A>C (p.Lys109Asn)	not specified [RCV005379871]	uncertain significance	3	26709999	26709999	Human		name
598250780	CV3988264	single nucleotide variant	NM_024727.4(LRRC31):c.703A>T (p.Ile235Phe)	not specified [RCV005366570]	uncertain significance	3	169856456	169856456	Human		name
598250825	CV3988282	single nucleotide variant	NM_018296.6(LRRC36):c.968A>G (p.Gln323Arg)	not specified [RCV005366577]	uncertain significance	16	67367230	67367230	Human		name
598250831	CV3988284	single nucleotide variant	NM_018296.6(LRRC36):c.424G>A (p.Ala142Thr)	not specified [RCV005366578]	uncertain significance	16	67347527	67347527	Human		name
598272936	CV3988291	single nucleotide variant	NM_018296.6(LRRC36):c.447G>C (p.Gln149His)	not specified [RCV005350595]	uncertain significance	16	67347550	67347550	Human		name
598272957	CV3988295	single nucleotide variant	NM_018296.6(LRRC36):c.664C>T (p.Arg222Cys)	not specified [RCV005350599]	uncertain significance	16	67363676	67363676	Human		name
617153848	CV4021202	single nucleotide variant	NM_014834.4(LRRC37A):c.2772A>G (p.Lys924=)	not provided [RCV005428955]	likely benign	17	46305527	46305527	Human		name
8625566	CV80690	single nucleotide variant	NM_024727.3(LRRC31):c.880G>A (p.Asp294Asn)	Malignant melanoma [RCV000060767]	not provided	3	169854924	169854924	Human		name
156369985	CV2194145	single nucleotide variant	NM_018296.6(LRRC36):c.1343G>C (p.Arg448Pro)	not specified [RCV004076896]	uncertain significance	16	67371091	67371091	Human		name
156182186	CV2201869	single nucleotide variant	NM_018296.6(LRRC36):c.1156C>A (p.Pro386Thr)	not specified [RCV004082295]	uncertain significance	16	67367418	67367418	Human		name
156376735	CV2206818	single nucleotide variant	NM_001195545.2(LRRC3C):c.94C>A (p.Leu32Ile)	not specified [RCV004083494]	uncertain significance	17	39944000	39944000	Human		name
156237410	CV2235678	single nucleotide variant	NM_199340.5(LRRC37A3):c.194C>A (p.Ser65Tyr)	not specified [RCV004111820]	uncertain significance	17	64897064	64897064	Human		name
155978186	CV2247006	single nucleotide variant	NM_024727.4(LRRC31):c.1024G>A (p.Glu342Lys)	not specified [RCV004114571]	uncertain significance	3	169851754	169851754	Human		name
156363432	CV2265731	single nucleotide variant	NM_018296.6(LRRC36):c.2087A>G (p.Asn696Ser)	not specified [RCV004124441]	uncertain significance	16	67384911	67384911	Human		name
156184092	CV2292205	single nucleotide variant	NM_024727.4(LRRC31):c.1030G>A (p.Asp344Asn)	not specified [RCV004148252]	uncertain significance	3	169851748	169851748	Human		name
155903109	CV2301577	single nucleotide variant	NM_018296.6(LRRC36):c.1757G>A (p.Arg586Lys)	not specified [RCV004162484]	uncertain significance	16	67376823	67376823	Human		name
156358710	CV2328057	single nucleotide variant	NM_018296.6(LRRC36):c.1172G>A (p.Gly391Glu)	not specified [RCV004173182]	uncertain significance	16	67367434	67367434	Human		name
156085527	CV2340424	single nucleotide variant	NM_018296.6(LRRC36):c.1291C>T (p.His431Tyr)	not specified [RCV004197152]	uncertain significance	16	67371039	67371039	Human		name
156364043	CV2341789	single nucleotide variant	NM_018296.6(LRRC36):c.1805T>C (p.Met602Thr)	not specified [RCV004184747]	uncertain significance	16	67376871	67376871	Human		name
156075399	CV2350876	single nucleotide variant	NM_018296.6(LRRC36):c.1697C>T (p.Pro566Leu)	not specified [RCV004211713]	uncertain significance	16	67376763	67376763	Human		name
156104395	CV2352448	single nucleotide variant	NM_199340.5(LRRC37A3):c.124T>C (p.Trp42Arg)	not specified [RCV004202957]	uncertain significance	17	64897134	64897134	Human		name
155930749	CV2362308	single nucleotide variant	NM_024727.4(LRRC31):c.1630A>C (p.Ile544Leu)	not specified [RCV004212944]	uncertain significance	3	169840011	169840011	Human		name
156199610	CV2392281	single nucleotide variant	NM_024727.4(LRRC31):c.1649G>A (p.Gly550Glu)	not specified [RCV004243886]	uncertain significance	3	169839992	169839992	Human		name
329391593	CV2448740	single nucleotide variant	NM_018296.6(LRRC36):c.1246G>A (p.Val416Ile)	not specified [RCV004259394]	uncertain significance	16	67370994	67370994	Human		name
329396516	CV2462585	single nucleotide variant	NM_024727.4(LRRC31):c.1139G>C (p.Ser380Thr)	not specified [RCV004278534]	uncertain significance	3	169851639	169851639	Human		name
401772160	CV2687433	single nucleotide variant	NM_024727.4(LRRC31):c.1199A>G (p.Asn400Ser)	not specified [RCV004300678]	uncertain significance	3	169848248	169848248	Human		name
401731595	CV2693892	single nucleotide variant	NM_024727.4(LRRC31):c.1376T>C (p.Leu459Pro)	not specified [RCV004300192]	uncertain significance	3	169840265	169840265	Human		name
401742747	CV2697854	single nucleotide variant	NM_001172779.2(LRRC34):c.77G>A (p.Arg26Lys)	not specified [RCV004300566]	uncertain significance	3	169812472	169812472	Human		name
401719547	CV2701169	single nucleotide variant	NM_199340.5(LRRC37A3):c.167C>T (p.Pro56Leu)	not specified [RCV004309749]	uncertain significance	17	64897091	64897091	Human		name
401736062	CV2703033	single nucleotide variant	NM_024727.4(LRRC31):c.1510C>T (p.His504Tyr)	not specified [RCV004321339]	uncertain significance	3	169840131	169840131	Human		name
401764565	CV2727988	single nucleotide variant	NM_199340.5(LRRC37A3):c.205C>T (p.Arg69Trp)	not specified [RCV004324141]	likely benign	17	64897053	64897053	Human		name
401882109	CV2784072	single nucleotide variant	NM_018296.6(LRRC36):c.1594C>T (p.Leu532Phe)	not specified [RCV004362472]	uncertain significance	16	67375346	67375346	Human		name
401877757	CV2786772	single nucleotide variant	NM_018296.6(LRRC36):c.1502C>T (p.Ser501Phe)	not specified [RCV004364178]	uncertain significance	16	67375254	67375254	Human		name
401914649	CV2808212	single nucleotide variant	NM_199340.5(LRRC37A3):c.2508C>T (p.Cys836=)	not provided [RCV003428409]	likely benign	17	64894750	64894750	Human		name
401905412	CV2813557	single nucleotide variant	NM_001128922.2(LRRC32):c.960G>A (p.Leu320=)	not provided [RCV003395924]	likely benign	11	76660633	76660633	Human		name
401905415	CV2813559	single nucleotide variant	NM_001128922.2(LRRC32):c.573C>T (p.Gly191=)	not provided [RCV003395925]	likely benign	11	76661020	76661020	Human		name
401935945	CV2818189	single nucleotide variant	NM_001105581.3(LRRC30):c.753C>G (p.Leu251=)	not provided [RCV003413409]	likely benign	18	7231891	7231891	Human		name
405655501	CV3277252	single nucleotide variant	NM_001105581.3(LRRC30):c.62C>T (p.Thr21Met)	not specified [RCV004415405]	uncertain significance	18	7231200	7231200	Human		name
405655507	CV3277255	single nucleotide variant	NM_024727.4(LRRC31):c.1004C>T (p.Pro335Leu)	not specified [RCV004415408]	uncertain significance	3	169851774	169851774	Human		name
405655509	CV3277256	single nucleotide variant	NM_024727.4(LRRC31):c.1331C>T (p.Ser444Leu)	not specified [RCV004415409]	uncertain significance	3	169840310	169840310	Human		name
405655511	CV3277257	single nucleotide variant	NM_024727.4(LRRC31):c.1432C>T (p.Arg478Trp)	not specified [RCV004415410]	likely benign	3	169840209	169840209	Human		name
405655556	CV3277277	single nucleotide variant	NM_001128922.2(LRRC32):c.29C>A (p.Ala10Asp)	not specified [RCV004415430]	uncertain significance	11	76665926	76665926	Human		name
405655583	CV3277293	single nucleotide variant	NM_018296.6(LRRC36):c.1321G>A (p.Gly441Arg)	not specified [RCV004415446]	uncertain significance	16	67371069	67371069	Human		name
405655584	CV3277294	single nucleotide variant	NM_018296.6(LRRC36):c.1334C>T (p.Thr445Ile)	not specified [RCV004415447]	uncertain significance	16	67371082	67371082	Human		name
405655586	CV3277295	single nucleotide variant	NM_018296.6(LRRC36):c.1828G>C (p.Val610Leu)	not specified [RCV004415448]	uncertain significance	16	67378610	67378610	Human		name
405655588	CV3277296	single nucleotide variant	NM_018296.6(LRRC36):c.1891G>C (p.Ala631Pro)	not specified [RCV004415449]	uncertain significance	16	67378673	67378673	Human		name
405655589	CV3277297	single nucleotide variant	NM_018296.6(LRRC36):c.1934A>T (p.Asp645Val)	not specified [RCV004415450]	uncertain significance	16	67382136	67382136	Human		name
405655592	CV3277298	single nucleotide variant	NM_018296.6(LRRC36):c.1967A>G (p.Gln656Arg)	not specified [RCV004415451]	uncertain significance	16	67382169	67382169	Human		name
405655593	CV3277299	single nucleotide variant	NM_018296.6(LRRC36):c.2089A>G (p.Lys697Glu)	not specified [RCV004415452]	uncertain significance	16	67384913	67384913	Human		name
405655699	CV3277341	single nucleotide variant	NM_199340.5(LRRC37A3):c.126G>C (p.Trp42Cys)	not specified [RCV004415494]	uncertain significance	17	64897132	64897132	Human		name
405655705	CV3277343	single nucleotide variant	NM_199340.5(LRRC37A3):c.201C>A (p.Phe67Leu)	not specified [RCV004415496]	likely benign	17	64897057	64897057	Human		name
405655712	CV3277346	single nucleotide variant	NM_199340.5(LRRC37A3):c.286C>G (p.Pro96Ala)	not specified [RCV004415499]	uncertain significance	17	64896972	64896972	Human		name
405655805	CV3277403	single nucleotide variant	NM_001195545.2(LRRC3C):c.86T>C (p.Leu29Pro)	not specified [RCV004415556]	uncertain significance	17	39943992	39943992	Human		name
407425646	CV3409558	single nucleotide variant	NM_001128922.2(LRRC32):c.579C>T (p.Phe193=)	not provided [RCV004585490]	likely benign	11	76661014	76661014	Human		name
407455883	CV3415770	single nucleotide variant	NM_001128922.2(LRRC32):c.882C>T (p.Ser294=)	not provided [RCV004598646]	likely benign	11	76660711	76660711	Human		name
407500744	CV3456439	single nucleotide variant	NM_001128922.2(LRRC32):c.74C>T (p.Pro25Leu)	not specified [RCV004644686]	uncertain significance	11	76665881	76665881	Human		name
407500774	CV3456452	single nucleotide variant	NM_018296.6(LRRC36):c.1456A>G (p.Asn486Asp)	not specified [RCV004644692]	uncertain significance	16	67371204	67371204	Human		name
407500777	CV3456453	single nucleotide variant	NM_018296.6(LRRC36):c.1754G>A (p.Cys585Tyr)	not specified [RCV004644693]	uncertain significance	16	67376820	67376820	Human		name
407500782	CV3456454	single nucleotide variant	NM_018296.6(LRRC36):c.1312G>A (p.Ala438Thr)	not specified [RCV004644694]	uncertain significance	16	67371060	67371060	Human		name
597778568	CV3693383	single nucleotide variant	NM_001010847.2(LRRC38):c.79G>A (p.Ala27Thr)	not specified [RCV004930163]	uncertain significance	1	13513515	13513515	Human		name
597625952	CV3696783	single nucleotide variant	NM_001105581.3(LRRC30):c.34G>T (p.Asp12Tyr)	not specified [RCV004938471]	uncertain significance	18	7231172	7231172	Human		name
597778502	CV3696785	single nucleotide variant	NM_024727.4(LRRC31):c.1018C>A (p.Leu340Ile)	not specified [RCV004930145]	uncertain significance	3	169851760	169851760	Human		name
597625958	CV3696786	single nucleotide variant	NM_024727.4(LRRC31):c.1401T>G (p.Asp467Glu)	not specified [RCV004938473]	uncertain significance	3	169840240	169840240	Human		name
597625965	CV3696788	single nucleotide variant	NM_024727.4(LRRC31):c.1216T>G (p.Cys406Gly)	not specified [RCV004938475]	uncertain significance	3	169848231	169848231	Human		name
597626157	CV3696804	single nucleotide variant	NM_001128922.2(LRRC32):c.96G>C (p.Lys32Asn)	not specified [RCV004938486]	uncertain significance	11	76661497	76661497	Human		name
597626131	CV3696814	single nucleotide variant	NM_018296.6(LRRC36):c.2232C>A (p.Ser744Arg)	not specified [RCV004938494]	uncertain significance	16	67385056	67385056	Human		name
597626125	CV3696816	single nucleotide variant	NM_018296.6(LRRC36):c.1484C>T (p.Thr495Ile)	not specified [RCV004938496]	uncertain significance	16	67371232	67371232	Human		name
597626117	CV3696818	single nucleotide variant	NM_018296.6(LRRC36):c.2234T>C (p.Val745Ala)	not specified [RCV004938498]	uncertain significance	16	67385058	67385058	Human		name
597778529	CV3696821	single nucleotide variant	NM_018296.6(LRRC36):c.1868T>A (p.Ile623Asn)	not specified [RCV004930151]	uncertain significance	16	67378650	67378650	Human		name
597626110	CV3696823	single nucleotide variant	NM_018296.6(LRRC36):c.1720T>G (p.Cys574Gly)	not specified [RCV004938500]	uncertain significance	16	67376786	67376786	Human		name
597626106	CV3696824	single nucleotide variant	NM_018296.6(LRRC36):c.1630G>A (p.Gly544Ser)	not specified [RCV004938501]	uncertain significance	16	67375382	67375382	Human		name
597625985	CV3696848	single nucleotide variant	NM_199340.5(LRRC37A3):c.203C>T (p.Pro68Leu)	not specified [RCV004938520]	uncertain significance	17	64897055	64897055	Human		name
598222317	CV3984689	single nucleotide variant	NM_001195545.2(LRRC3C):c.74C>T (p.Thr25Ile)	not specified [RCV005379873]	uncertain significance	17	39943980	39943980	Human		name
598272873	CV3988265	single nucleotide variant	NM_024727.4(LRRC31):c.1035A>C (p.Leu345Phe)	not specified [RCV005350583]	uncertain significance	3	169851743	169851743	Human		name
598250787	CV3988266	single nucleotide variant	NM_024727.4(LRRC31):c.1480A>G (p.Asn494Asp)	not specified [RCV005366571]	uncertain significance	3	169840161	169840161	Human		name
598272885	CV3988268	single nucleotide variant	NM_024727.4(LRRC31):c.1331C>G (p.Ser444Trp)	not specified [RCV005350585]	uncertain significance	3	169840310	169840310	Human		name
598272919	CV3988283	single nucleotide variant	NM_018296.6(LRRC36):c.1741A>G (p.Met581Val)	not specified [RCV005350592]	uncertain significance	16	67376807	67376807	Human		name
598272932	CV3988289	single nucleotide variant	NM_018296.6(LRRC36):c.1743G>T (p.Met581Ile)	not specified [RCV005350594]	uncertain significance	16	67376809	67376809	Human		name
598250850	CV3988290	single nucleotide variant	NM_018296.6(LRRC36):c.1963A>G (p.Met655Val)	not specified [RCV005366582]	uncertain significance	16	67382165	67382165	Human		name
598272941	CV3988292	single nucleotide variant	NM_018296.6(LRRC36):c.1570C>T (p.His524Tyr)	not specified [RCV005350596]	uncertain significance	16	67375322	67375322	Human		name
598272946	CV3988293	single nucleotide variant	NM_018296.6(LRRC36):c.1445T>C (p.Leu482Pro)	not specified [RCV005350597]	uncertain significance	16	67371193	67371193	Human		name
598272952	CV3988294	single nucleotide variant	NM_018296.6(LRRC36):c.1573G>A (p.Val525Met)	not specified [RCV005350598]	uncertain significance	16	67375325	67375325	Human		name
598250857	CV3988296	single nucleotide variant	NM_018296.6(LRRC36):c.1618T>G (p.Trp540Gly)	not specified [RCV005366583]	uncertain significance	16	67375370	67375370	Human		name
598273005	CV3988322	single nucleotide variant	NM_199340.5(LRRC37A3):c.259C>G (p.Leu87Val)	not specified [RCV005350608]	uncertain significance	17	64896999	64896999	Human		name
598273009	CV3988323	single nucleotide variant	NM_199340.5(LRRC37A3):c.230T>C (p.Leu77Pro)	not specified [RCV005350609]	likely benign	17	64897028	64897028	Human		name
8634381	CV89601	single nucleotide variant	NM_001128922.1(LRRC32):c.774C>T (p.Phe258=)	Malignant melanoma [RCV000069698]	not provided	11	76660819	76660819	Human		name
8636079	CV91302	single nucleotide variant	NM_052888.2(LRRC37B):c.563C>T (p.Ser188Leu)	Malignant melanoma [RCV000071400]	not provided	17	32021709	32021709	Human		name
153304458	CV1687074	single nucleotide variant	NM_001128922.2(LRRC32):c.1728C>T (p.Cys576=)	not provided [RCV002262362]	likely benign	11	76659865	76659865	Human		name
156138299	CV2202811	single nucleotide variant	NM_199340.5(LRRC37A3):c.985T>C (p.Phe329Leu)	not specified [RCV004073669]	uncertain significance	17	64896273	64896273	Human		name
156071015	CV2232559	single nucleotide variant	NM_014834.4(LRRC37A):c.2360T>C (p.Leu787Pro)	not specified [RCV004099155]	uncertain significance	17	46297493	46297493	Human		name
156025393	CV2242232	single nucleotide variant	NM_001105581.3(LRRC30):c.151G>A (p.Val51Ile)	not specified [RCV004111260]	uncertain significance	18	7231289	7231289	Human		name
156053937	CV2243024	single nucleotide variant	NM_014834.4(LRRC37A):c.2923C>A (p.Pro975Thr)	not specified [RCV004109944]	uncertain significance	17	46322338	46322338	Human		name
155981303	CV2244059	single nucleotide variant	NM_014834.4(LRRC37A):c.2189A>T (p.Lys730Ile)	not specified [RCV004108538]	uncertain significance	17	46297322	46297322	Human		name
156214979	CV2257531	single nucleotide variant	NM_199340.5(LRRC37A3):c.996G>T (p.Glu332Asp)	not specified [RCV004125586]	uncertain significance	17	64896262	64896262	Human		name
156021483	CV2264461	single nucleotide variant	NM_001105581.3(LRRC30):c.283C>T (p.Arg95Trp)	not specified [RCV004138356]	uncertain significance	18	7231421	7231421	Human		name
156236923	CV2268305	single nucleotide variant	NM_001010847.2(LRRC38):c.262A>G (p.Arg88Gly)	not specified [RCV004138594]	uncertain significance	1	13513332	13513332	Human		name
156011263	CV2291126	single nucleotide variant	NM_001172779.2(LRRC34):c.110C>G (p.Thr37Ser)	not specified [RCV004151649]	uncertain significance	3	169812439	169812439	Human		name
156196825	CV2293501	single nucleotide variant	NM_014834.4(LRRC37A):c.2396C>G (p.Pro799Arg)	not specified [RCV004153038]	uncertain significance	17	46297529	46297529	Human		name
155904507	CV2298816	single nucleotide variant	NM_001105581.3(LRRC30):c.137G>A (p.Arg46Gln)	not specified [RCV004156368]	uncertain significance	18	7231275	7231275	Human		name
156209544	CV2304516	single nucleotide variant	NM_199340.5(LRRC37A3):c.814A>G (p.Ser272Gly)	not specified [RCV004164597]	uncertain significance	17	64896444	64896444	Human		name
156162426	CV2311816	single nucleotide variant	NM_001195545.2(LRRC3C):c.116G>A (p.Gly39Glu)	not specified [RCV004170665]	uncertain significance	17	39944022	39944022	Human		name
156060192	CV2323072	single nucleotide variant	NM_014834.4(LRRC37A):c.2771A>T (p.Lys924Ile)	not specified [RCV004187491]	uncertain significance	17	46305526	46305526	Human		name
156351598	CV2323791	single nucleotide variant	NM_014834.4(LRRC37A):c.2471C>T (p.Ala824Val)	not specified [RCV004176336]	uncertain significance	17	46297604	46297604	Human		name
155964696	CV2330480	single nucleotide variant	NM_199340.5(LRRC37A3):c.541C>A (p.Gln181Lys)	not specified [RCV004181047]	uncertain significance	17	64896717	64896717	Human		name
155918170	CV2332948	single nucleotide variant	NM_199340.5(LRRC37A3):c.475A>G (p.Ser159Gly)	not specified [RCV004192202]	uncertain significance	17	64896783	64896783	Human		name
156068522	CV2341050	single nucleotide variant	NM_001195545.2(LRRC3C):c.181C>T (p.Arg61Trp)	not specified [RCV004181533]	uncertain significance	17	39944087	39944087	Human		name
156087012	CV2341145	single nucleotide variant	NM_001105581.3(LRRC30):c.139G>A (p.Gly47Ser)	not specified [RCV004181621]	uncertain significance	18	7231277	7231277	Human		name
155981518	CV2351351	single nucleotide variant	NM_199340.5(LRRC37A3):c.310G>A (p.Glu104Lys)	not specified [RCV004193051]	uncertain significance	17	64896948	64896948	Human		name
156009660	CV2362025	single nucleotide variant	NM_199340.5(LRRC37A3):c.577G>A (p.Gly193Ser)	not specified [RCV004209837]	uncertain significance	17	64896681	64896681	Human		name
156382995	CV2363095	single nucleotide variant	NM_001010847.2(LRRC38):c.127C>T (p.Arg43Cys)	not specified [RCV004211221]	uncertain significance	1	13513467	13513467	Human		name
155930218	CV2366625	single nucleotide variant	NM_001195545.2(LRRC3C):c.178G>A (p.Glu60Lys)	not specified [RCV004210638]	uncertain significance	17	39944084	39944084	Human		name
155908868	CV2387459	single nucleotide variant	NM_199340.5(LRRC37A3):c.590C>T (p.Pro197Leu)	not specified [RCV004240324]	likely benign	17	64896668	64896668	Human		name
156110552	CV2387658	single nucleotide variant	NM_001105581.3(LRRC30):c.118C>G (p.Pro40Ala)	not specified [RCV004234204]	uncertain significance	18	7231256	7231256	Human		name
156252214	CV2390012	single nucleotide variant	NM_014834.4(LRRC37A):c.2320G>A (p.Ala774Thr)	not specified [RCV004238627]	uncertain significance	17	46297453	46297453	Human		name
156085256	CV2390553	single nucleotide variant	NM_014834.4(LRRC37A):c.2480G>A (p.Ser827Asn)	not specified [RCV004239085]	likely benign	17	46297613	46297613	Human		name
156085591	CV2390637	single nucleotide variant	NM_014834.4(LRRC37A):c.2335C>T (p.Arg779Trp)	not specified [RCV004239158]	uncertain significance	17	46297468	46297468	Human		name
156200709	CV2392426	single nucleotide variant	NM_014834.4(LRRC37A):c.2572C>T (p.Pro858Ser)	not specified [RCV004244007]	likely benign	17	46297705	46297705	Human		name
156115293	CV2397269	single nucleotide variant	NM_014834.4(LRRC37A):c.2803C>T (p.Pro935Ser)	not specified [RCV004238802]	likely benign	17	46305558	46305558	Human		name
156160940	CV2398230	single nucleotide variant	NM_001128922.2(LRRC32):c.134C>T (p.Ser45Leu)	not specified [RCV004235144]	likely benign	11	76661459	76661459	Human		name
329349613	CV2438155	single nucleotide variant	NM_014834.4(LRRC37A):c.2158C>T (p.Pro720Ser)	not specified [RCV004256932]	uncertain significance	17	46297291	46297291	Human		name
329402371	CV2454214	single nucleotide variant	NM_199340.5(LRRC37A3):c.827C>T (p.Pro276Leu)	not specified [RCV004265695]	uncertain significance	17	64896431	64896431	Human		name
329349972	CV2457172	single nucleotide variant	NM_014834.4(LRRC37A):c.2323C>T (p.Pro775Ser)	not specified [RCV004265258]	uncertain significance	17	46297456	46297456	Human		name
329349979	CV2457931	single nucleotide variant	NM_014834.4(LRRC37A):c.2113A>G (p.Lys705Glu)	not specified [RCV004271516]	uncertain significance	17	46297246	46297246	Human		name
329376529	CV2472133	single nucleotide variant	NM_001105581.3(LRRC30):c.178A>G (p.Met60Val)	not specified [RCV004283262]	uncertain significance	18	7231316	7231316	Human		name
401737924	CV2676068	single nucleotide variant	NM_001321350.2(LRRC37B):c.70G>A (p.Glu24Lys)	not specified [RCV004284296]	uncertain significance	17	32021462	32021462	Human		name
401779283	CV2709663	single nucleotide variant	NM_199340.5(LRRC37A3):c.463G>C (p.Ala155Pro)	not specified [RCV004318875]	uncertain significance	17	64896795	64896795	Human		name
401738224	CV2714370	single nucleotide variant	NM_001105581.3(LRRC30):c.170C>T (p.Thr57Met)	not specified [RCV004317905]	uncertain significance	18	7231308	7231308	Human		name
401752000	CV2723084	single nucleotide variant	NM_001105581.3(LRRC30):c.101T>G (p.Leu34Arg)	not specified [RCV004327561]	uncertain significance	18	7231239	7231239	Human		name
401745103	CV2725284	single nucleotide variant	NM_014834.4(LRRC37A):c.2917C>A (p.His973Asn)	not specified [RCV004319949]	uncertain significance	17	46322332	46322332	Human		name
401890676	CV2775725	single nucleotide variant	NM_001172779.2(LRRC34):c.255G>T (p.Lys85Asn)	not specified [RCV004350851]	uncertain significance	3	169808630	169808630	Human		name
401906502	CV2808211	single nucleotide variant	NM_199340.5(LRRC37A3):c.4029G>A (p.Pro1343=)	not provided [RCV003421424]	likely benign	17	64860117	64860117	Human		name
401905408	CV2813554	single nucleotide variant	NM_001128922.2(LRRC32):c.1719C>T (p.Leu573=)	not provided [RCV003395922]	likely benign	11	76659874	76659874	Human		name
401905411	CV2813555	single nucleotide variant	NM_001128922.2(LRRC32):c.1456T>C (p.Leu486=)	not provided [RCV003395923]	likely benign	11	76660137	76660137	Human		name
401929088	CV2813556	single nucleotide variant	NM_001128922.2(LRRC32):c.1191C>T (p.Ala397=)	not provided [RCV003390093]	likely benign	11	76660402	76660402	Human		name
405655492	CV3277248	single nucleotide variant	NM_001105581.3(LRRC30):c.280A>G (p.Thr94Ala)	not specified [RCV004415401]	uncertain significance	18	7231418	7231418	Human		name
405655497	CV3277250	single nucleotide variant	NM_001105581.3(LRRC30):c.292G>A (p.Val98Ile)	not specified [RCV004415403]	uncertain significance	18	7231430	7231430	Human		name
405655539	CV3277270	single nucleotide variant	NM_001128922.2(LRRC32):c.112C>A (p.Leu38Met)	not specified [RCV004415423]	uncertain significance	11	76661481	76661481	Human		name
405655554	CV3277276	single nucleotide variant	NM_001128922.2(LRRC32):c.249T>G (p.Asn83Lys)	not specified [RCV004415429]	uncertain significance	11	76661344	76661344	Human		name
405655573	CV3277287	single nucleotide variant	NM_001172779.2(LRRC34):c.209C>T (p.Pro70Leu)	not specified [RCV004415440]	uncertain significance	3	169808676	169808676	Human		name
405655600	CV3277303	single nucleotide variant	NM_014834.4(LRRC37A):c.2299A>G (p.Thr767Ala)	not specified [RCV004415456]	uncertain significance	17	46297432	46297432	Human		name
405655602	CV3277304	single nucleotide variant	NM_014834.4(LRRC37A):c.2338G>C (p.Val780Leu)	not specified [RCV004415457]	likely benign	17	46297471	46297471	Human		name
405655604	CV3277305	single nucleotide variant	NM_014834.4(LRRC37A):c.2387A>T (p.Glu796Val)	not specified [RCV004415458]	uncertain significance	17	46297520	46297520	Human		name
405655606	CV3277306	single nucleotide variant	NM_014834.4(LRRC37A):c.2398G>A (p.Ala800Thr)	not specified [RCV004415459]	likely benign	17	46297531	46297531	Human		name
405655609	CV3277307	single nucleotide variant	NM_014834.4(LRRC37A):c.2993C>G (p.Thr998Arg)	not specified [RCV004415460]	uncertain significance	17	46322967	46322967	Human		name
405655722	CV3277352	single nucleotide variant	NM_199340.5(LRRC37A3):c.358C>T (p.Pro120Ser)	not specified [RCV004415505]	uncertain significance	17	64896900	64896900	Human		name
405655740	CV3277363	single nucleotide variant	NM_199340.5(LRRC37A3):c.947C>A (p.Thr316Lys)	not specified [RCV004415516]	uncertain significance	17	64896311	64896311	Human		name
405655772	CV3277383	single nucleotide variant	NM_001010847.2(LRRC38):c.175C>T (p.Arg59Cys)	not specified [RCV004415536]	uncertain significance	1	13513419	13513419	Human		name
405655774	CV3277384	single nucleotide variant	NM_001010847.2(LRRC38):c.176G>A (p.Arg59His)	not specified [RCV004415537]	uncertain significance	1	13513418	13513418	Human		name
405655799	CV3277399	single nucleotide variant	NM_001195545.2(LRRC3C):c.226G>A (p.Gly76Ser)	not specified [RCV004415552]	uncertain significance	17	39944132	39944132	Human		name
407456165	CV3415817	single nucleotide variant	NM_001128922.2(LRRC32):c.1467G>C (p.Leu489=)	not provided [RCV004598694]	likely benign	11	76660126	76660126	Human		name
407468141	CV3456448	single nucleotide variant	NM_001172779.2(LRRC34):c.292A>T (p.Asn98Tyr)	not specified [RCV004636166]	uncertain significance	3	169807675	169807675	Human		name
407484077	CV3456458	single nucleotide variant	NM_014834.4(LRRC37A):c.2345C>G (p.Thr782Ser)	not specified [RCV004636169]	uncertain significance	17	46297478	46297478	Human		name
407485160	CV3456460	single nucleotide variant	NM_014834.4(LRRC37A):c.2381C>T (p.Pro794Leu)	not specified [RCV004644698]	uncertain significance	17	46297514	46297514	Human		name
407485482	CV3456461	single nucleotide variant	NM_014834.4(LRRC37A):c.2125C>G (p.Gln709Glu)	not specified [RCV004644699]	uncertain significance	17	46297258	46297258	Human		name
407468151	CV3456472	single nucleotide variant	NM_199340.5(LRRC37A3):c.598C>T (p.Arg200Trp)	not specified [RCV004636172]	uncertain significance	17	64896660	64896660	Human		name
407500799	CV3456473	single nucleotide variant	NM_199340.5(LRRC37A3):c.426G>T (p.Arg142Ser)	not specified [RCV004644709]	uncertain significance	17	64896832	64896832	Human		name
407500815	CV3456476	single nucleotide variant	NM_199340.5(LRRC37A3):c.998T>C (p.Val333Ala)	not specified [RCV004644712]	uncertain significance	17	64896260	64896260	Human		name
407500890	CV3456499	single nucleotide variant	NM_001195545.2(LRRC3C):c.175G>C (p.Gly59Arg)	not specified [RCV004644732]	uncertain significance	17	39944081	39944081	Human		name
407500895	CV3456500	single nucleotide variant	NM_001195545.2(LRRC3C):c.244C>T (p.Arg82Cys)	not specified [RCV004644733]	uncertain significance	17	39944150	39944150	Human		name
597626188	CV3693391	single nucleotide variant	NM_001195545.2(LRRC3C):c.119G>A (p.Gly40Asp)	not specified [RCV004938556]	uncertain significance	17	39944025	39944025	Human		name
597778576	CV3693392	single nucleotide variant	NM_001195545.2(LRRC3C):c.146C>T (p.Pro49Leu)	not specified [RCV004930165]	uncertain significance	17	39944052	39944052	Human		name
597626192	CV3693394	single nucleotide variant	NM_001195545.2(LRRC3C):c.245G>A (p.Arg82His)	not specified [RCV004938557]	uncertain significance	17	39944151	39944151	Human		name
597778580	CV3693395	single nucleotide variant	NM_001195545.2(LRRC3C):c.190C>T (p.Arg64Cys)	not specified [RCV004930166]	uncertain significance	17	39944096	39944096	Human		name
597626199	CV3693397	single nucleotide variant	NM_001195545.2(LRRC3C):c.115G>A (p.Gly39Arg)	not specified [RCV004938559]	uncertain significance	17	39944021	39944021	Human		name
597625941	CV3696780	single nucleotide variant	NM_001105581.3(LRRC30):c.221A>C (p.Gln74Pro)	not specified [RCV004938468]	uncertain significance	18	7231359	7231359	Human		name
597778510	CV3696799	single nucleotide variant	NM_001128922.2(LRRC32):c.185G>A (p.Arg62Gln)	not specified [RCV004930147]	likely benign	11	76661408	76661408	Human		name
597626134	CV3696813	single nucleotide variant	NM_001172779.2(LRRC34):c.208C>A (p.Pro70Thr)	not specified [RCV004938493]	uncertain significance	3	169808677	169808677	Human		name
597697455	CV3696827	single nucleotide variant	NM_014834.4(LRRC37A):c.2389C>G (p.Leu797Val)	not specified [RCV004938504]	likely benign	17	46297522	46297522	Human		name
597695846	CV3696830	single nucleotide variant	NM_014834.4(LRRC37A):c.2432C>T (p.Thr811Ile)	not specified [RCV004930152]	uncertain significance	17	46297565	46297565	Human		name
597697425	CV3696831	single nucleotide variant	NM_014834.4(LRRC37A):c.2380C>T (p.Pro794Ser)	not specified [RCV004938507]	uncertain significance	17	46297513	46297513	Human		name
597625991	CV3696851	single nucleotide variant	NM_199340.5(LRRC37A3):c.551A>T (p.Tyr184Phe)	not specified [RCV004938522]	uncertain significance	17	64896707	64896707	Human		name
597778541	CV3696865	single nucleotide variant	NM_199340.5(LRRC37A3):c.964C>G (p.Gln322Glu)	not specified [RCV004930157]	uncertain significance	17	64896294	64896294	Human		name
597626082	CV3696889	single nucleotide variant	NM_001010847.2(LRRC38):c.123C>G (p.Asp41Glu)	not specified [RCV004938549]	uncertain significance	1	13513471	13513471	Human		name
598273034	CV3984670	single nucleotide variant	NM_001321350.2(LRRC37B):c.64G>T (p.Ala22Ser)	not specified [RCV005350615]	uncertain significance	17	32021456	32021456	Human		name
598273057	CV3984680	single nucleotide variant	NM_001010847.2(LRRC38):c.133C>A (p.Arg45Ser)	not specified [RCV005350621]	uncertain significance	1	13513461	13513461	Human		name
598251021	CV3984691	single nucleotide variant	NM_001195545.2(LRRC3C):c.176G>A (p.Gly59Asp)	not specified [RCV005366609]	uncertain significance	17	39944082	39944082	Human		name
598250774	CV3988262	single nucleotide variant	NM_001105581.3(LRRC30):c.211T>C (p.Ser71Pro)	not specified [RCV005366569]	uncertain significance	18	7231349	7231349	Human		name
598231538	CV3988298	single nucleotide variant	NM_014834.4(LRRC37A):c.2336G>A (p.Arg779Gln)	not specified [RCV005362881]	likely benign	17	46297469	46297469	Human		name
598250869	CV3988299	single nucleotide variant	NM_014834.4(LRRC37A):c.2168T>C (p.Leu723Pro)	not specified [RCV005366585]	uncertain significance	17	46297301	46297301	Human		name
15162418	CV704296	single nucleotide variant	NM_199340.5(LRRC37A3):c.4113T>C (p.Pro1371=)	not provided [RCV000947850]	benign	17	64860033	64860033	Human		name
15162430	CV704298	single nucleotide variant	NM_199340.5(LRRC37A3):c.3207G>A (p.Ala1069=)	not provided [RCV000947852]	benign	17	64860939	64860939	Human		name
15127179	CV738299	single nucleotide variant	NM_001128922.2(LRRC32):c.1320C>T (p.Ser440=)	not provided [RCV000897062]	benign	11	76660273	76660273	Human		name
15171899	CV740959	single nucleotide variant	NM_199340.5(LRRC37A3):c.4347C>T (p.Asn1449=)	not provided [RCV000905560]	benign	17	64859799	64859799	Human		name
8630683	CV85838	single nucleotide variant	NM_001172779.1(LRRC34):c.244G>A (p.Glu82Lys)	Malignant melanoma [RCV000065921]	not provided	3	169808641	169808641	Human		name
34892104	CV906275	single nucleotide variant	NM_001172779.2(LRRC34):c.199A>T (p.Lys67Ter)	Joubert syndrome [RCV001175214]	uncertain significance	3	169808686	169808686	Human	1	name
8635860	CV91083	single nucleotide variant	NM_001161575.1(LRRC36):c.128C>T (p.Ser43Phe)	Malignant melanoma [RCV000071181]	not provided	16	67350204	67350204	Human		name
8636294	CV91517	single nucleotide variant	NM_199340.3(LRRC37A3):c.4455C>T (p.Ile1485=)	Malignant melanoma [RCV000071615]	not provided	17	64859691	64859691	Human		name
8636296	CV91519	single nucleotide variant	NM_199340.3(LRRC37A3):c.3120G>A (p.Lys1040=)	Malignant melanoma [RCV000071617]	not provided	17	64862952	64862952	Human		name
151234511	CV1320984	single nucleotide variant	NM_001128922.2(LRRC32):c.980T>C (p.Ile327Thr)	Cleft palate, proliferative retinopathy, and developmental delay [RCV001801335]	likely pathogenic	11	76660613	76660613	Human	1	name
151880884	CV1406024	single nucleotide variant	NM_001172779.2(LRRC34):c.890G>A (p.Arg297His)	not provided [RCV001941015]	uncertain significance	3	169796763	169796763	Human		name
9687173	CV171608	deletion	NM_199340.5(LRRC37A3):c.3859del (p.Ala1287fs)	Prostate cancer [RCV000149392]	uncertain significance	17	64860287	64860287	Human	2	name
156365386	CV2193189	single nucleotide variant	NM_014834.4(LRRC37A):c.4628C>T (p.Thr1543Met)	not specified [RCV004071180]	uncertain significance	17	46331905	46331905	Human		name
155963908	CV2194192	single nucleotide variant	NM_001172779.2(LRRC34):c.702C>A (p.Asn234Lys)	not specified [RCV004077273]	uncertain significance	3	169800710	169800710	Human		name
156325037	CV2195133	single nucleotide variant	NM_014834.4(LRRC37A):c.4940C>T (p.Pro1647Leu)	not specified [RCV004078038]	uncertain significance	17	46337454	46337454	Human		name
156147717	CV2196981	single nucleotide variant	NM_001105581.3(LRRC30):c.618G>C (p.Gln206His)	not specified [RCV004071436]	uncertain significance	18	7231756	7231756	Human		name
156324610	CV2198794	single nucleotide variant	NM_199340.5(LRRC37A3):c.1868C>T (p.Thr623Met)	not specified [RCV004077838]	uncertain significance	17	64895390	64895390	Human		name
156400158	CV2199009	single nucleotide variant	NM_199340.5(LRRC37A3):c.2530A>T (p.Ile844Phe)	not specified [RCV004080417]	uncertain significance	17	64894728	64894728	Human		name
156373373	CV2201130	single nucleotide variant	NM_199340.5(LRRC37A3):c.1030A>G (p.Ile344Val)	not specified [RCV004077292]	uncertain significance	17	64896228	64896228	Human		name
155915178	CV2204029	single nucleotide variant	NM_199340.5(LRRC37A3):c.1892C>T (p.Pro631Leu)	not specified [RCV004070067]	likely benign	17	64895366	64895366	Human		name
156372787	CV2204565	single nucleotide variant	NM_001195545.2(LRRC3C):c.319G>A (p.Glu107Lys)	not specified [RCV004081676]	uncertain significance	17	39944225	39944225	Human		name
156189290	CV2205927	single nucleotide variant	NM_001172779.2(LRRC34):c.496G>A (p.Glu166Lys)	not specified [RCV004078358]	uncertain significance	3	169806880	169806880	Human		name
156279838	CV2206318	single nucleotide variant	NM_001195545.2(LRRC3C):c.502C>T (p.Leu168Phe)	not specified [RCV004078658]	uncertain significance	17	39944408	39944408	Human		name
156280570	CV2206413	single nucleotide variant	NM_001105581.3(LRRC30):c.791C>T (p.Pro264Leu)	not specified [RCV004078735]	uncertain significance	18	7231929	7231929	Human		name
156138488	CV2211922	single nucleotide variant	NM_014834.4(LRRC37A):c.4394T>C (p.Leu1465Ser)	not specified [RCV004087052]	uncertain significance	17	46331671	46331671	Human		name
156039009	CV2215077	single nucleotide variant	NM_199340.5(LRRC37A3):c.1312G>A (p.Ala438Thr)	not specified [RCV004084846]	uncertain significance	17	64895946	64895946	Human		name
156105717	CV2217674	single nucleotide variant	NM_001128922.2(LRRC32):c.742C>G (p.Leu248Val)	not specified [RCV004083868]	uncertain significance	11	76660851	76660851	Human		name
156112148	CV2218016	single nucleotide variant	NM_199340.5(LRRC37A3):c.1744C>G (p.Leu582Val)	not specified [RCV004086461]	uncertain significance	17	64895514	64895514	Human		name
155917413	CV2236542	single nucleotide variant	NM_199340.5(LRRC37A3):c.1666G>A (p.Glu556Lys)	not specified [RCV004110538]	uncertain significance	17	64895592	64895592	Human		name
155952415	CV2238959	single nucleotide variant	NM_199340.5(LRRC37A3):c.1145C>T (p.Thr382Ile)	not specified [RCV004109853]	uncertain significance	17	64896113	64896113	Human		name
155952424	CV2238960	single nucleotide variant	NM_199340.5(LRRC37A3):c.2439T>G (p.Asn813Lys)	not specified [RCV004109854]	uncertain significance	17	64894819	64894819	Human		name
155916420	CV2239733	single nucleotide variant	NM_014834.4(LRRC37A):c.4369G>A (p.Glu1457Lys)	not specified [RCV004108269]	likely benign	17	46331646	46331646	Human		name
156185688	CV2251705	single nucleotide variant	NM_199340.5(LRRC37A3):c.1013C>G (p.Thr338Ser)	not specified [RCV004119716]	uncertain significance	17	64896245	64896245	Human		name
156204023	CV2252455	single nucleotide variant	NM_001172779.2(LRRC34):c.363T>A (p.Asn121Lys)	not specified [RCV004116576]	likely benign	3	169807604	169807604	Human		name
156089018	CV2259095	single nucleotide variant	NM_001010847.2(LRRC38):c.494G>A (p.Arg165His)	not specified [RCV004120350]	uncertain significance	1	13513100	13513100	Human		name
156197251	CV2259247	single nucleotide variant	NM_199340.5(LRRC37A3):c.2422G>A (p.Glu808Lys)	not specified [RCV004122269]	uncertain significance	17	64894836	64894836	Human		name
156104011	CV2260543	single nucleotide variant	NM_199340.5(LRRC37A3):c.1861C>G (p.Pro621Ala)	not specified [RCV004123322]	uncertain significance	17	64895397	64895397	Human		name
156110587	CV2261632	single nucleotide variant	NM_199340.5(LRRC37A3):c.2291G>A (p.Gly764Glu)	not specified [RCV004125957]	uncertain significance	17	64894967	64894967	Human		name
155979384	CV2266626	single nucleotide variant	NM_001105581.3(LRRC30):c.869T>C (p.Met290Thr)	not specified [RCV004131168]	uncertain significance	18	7232007	7232007	Human		name
156364847	CV2272005	single nucleotide variant	NM_001172779.2(LRRC34):c.733C>T (p.Pro245Ser)	not specified [RCV004124812]	uncertain significance	3	169800679	169800679	Human		name
156025704	CV2274006	single nucleotide variant	NM_014834.4(LRRC37A):c.3350T>C (p.Ile1117Thr)	not specified [RCV004134394]	uncertain significance	17	46330627	46330627	Human		name
155958962	CV2278388	single nucleotide variant	NM_001105581.3(LRRC30):c.823C>G (p.Pro275Ala)	not specified [RCV004132849]	uncertain significance	18	7231961	7231961	Human		name
156030226	CV2278698	single nucleotide variant	NM_014834.4(LRRC37A):c.3619A>G (p.Thr1207Ala)	not specified [RCV004134892]	uncertain significance	17	46330896	46330896	Human		name
155917327	CV2278700	single nucleotide variant	NM_014834.4(LRRC37A):c.3620C>G (p.Thr1207Arg)	not specified [RCV004134894]	likely benign	17	46330897	46330897	Human		name
155916342	CV2282029	single nucleotide variant	NM_199340.5(LRRC37A3):c.2051C>T (p.Thr684Ile)	not specified [RCV004138783]	uncertain significance	17	64895207	64895207	Human		name
155958754	CV2282250	single nucleotide variant	NM_001128922.2(LRRC32):c.788C>G (p.Ala263Gly)	not specified [RCV004132824]	uncertain significance	11	76660805	76660805	Human		name
155906176	CV2283392	single nucleotide variant	NM_001172779.2(LRRC34):c.298C>G (p.Arg100Gly)	not specified [RCV004146038]	uncertain significance	3	169807669	169807669	Human		name
155988379	CV2285375	single nucleotide variant	NM_001105581.3(LRRC30):c.842C>T (p.Pro281Leu)	not specified [RCV004139243]	uncertain significance	18	7231980	7231980	Human		name
156290465	CV2296507	single nucleotide variant	NM_014834.4(LRRC37A):c.3799C>A (p.Gln1267Lys)	not specified [RCV004154586]	uncertain significance	17	46331076	46331076	Human		name
156291033	CV2296586	single nucleotide variant	NM_014834.4(LRRC37A):c.3663G>C (p.Gln1221His)	not specified [RCV004154651]	uncertain significance	17	46330940	46330940	Human		name
155970052	CV2309144	single nucleotide variant	NM_001105581.3(LRRC30):c.305G>C (p.Cys102Ser)	not specified [RCV004171498]	uncertain significance	18	7231443	7231443	Human		name
156210486	CV2309720	single nucleotide variant	NM_199340.5(LRRC37A3):c.2351A>T (p.His784Leu)	not specified [RCV004160851]	uncertain significance	17	64894907	64894907	Human		name
156053362	CV2312448	single nucleotide variant	NM_199340.5(LRRC37A3):c.1324C>T (p.Leu442Phe)	not specified [RCV004167129]	uncertain significance	17	64895934	64895934	Human		name
156109047	CV2313913	single nucleotide variant	NM_001172779.2(LRRC34):c.631A>G (p.Lys211Glu)	not specified [RCV004164223]	uncertain significance	3	169804079	169804079	Human		name
156268497	CV2314790	single nucleotide variant	NM_001172779.2(LRRC34):c.764C>T (p.Thr255Ile)	not specified [RCV004170921]	uncertain significance	3	169796889	169796889	Human		name
156350917	CV2316305	single nucleotide variant	NM_001128922.2(LRRC32):c.625C>A (p.Leu209Ile)	not specified [RCV004174326]	uncertain significance	11	76660968	76660968	Human		name
156171444	CV2317210	single nucleotide variant	NM_001172779.2(LRRC34):c.661A>G (p.Met221Val)	not specified [RCV004176566]	uncertain significance	3	169800751	169800751	Human		name
156296236	CV2318125	single nucleotide variant	NM_001105581.3(LRRC30):c.661A>T (p.Ile221Phe)	not specified [RCV004177538]	uncertain significance	18	7231799	7231799	Human		name
156163807	CV2319659	single nucleotide variant	NM_014834.4(LRRC37A):c.4114T>A (p.Phe1372Ile)	not specified [RCV004185204]	uncertain significance	17	46331391	46331391	Human		name
156059637	CV2323029	single nucleotide variant	NM_199340.5(LRRC37A3):c.1052T>C (p.Met351Thr)	not specified [RCV004185454]	uncertain significance	17	64896206	64896206	Human		name
156268516	CV2326306	single nucleotide variant	NM_001195545.2(LRRC3C):c.701C>T (p.Thr234Ile)	not specified [RCV004180853]	uncertain significance	17	39944607	39944607	Human		name
156326528	CV2331961	single nucleotide variant	NM_001010847.2(LRRC38):c.868G>A (p.Glu290Lys)	not specified [RCV004189021]	uncertain significance	1	13475863	13475863	Human		name
156186716	CV2332607	single nucleotide variant	NM_001010847.2(LRRC38):c.838G>A (p.Ala280Thr)	not specified [RCV004189289]	uncertain significance	1	13475893	13475893	Human		name
156285056	CV2334813	single nucleotide variant	NM_001128922.2(LRRC32):c.341C>T (p.Ala114Val)	not specified [RCV004181925]	uncertain significance	11	76661252	76661252	Human		name
155980375	CV2336906	single nucleotide variant	NM_001195545.2(LRRC3C):c.586G>A (p.Val196Met)	not specified [RCV004190521]	uncertain significance	17	39944492	39944492	Human		name
156332460	CV2339785	single nucleotide variant	NM_001010847.2(LRRC38):c.383G>A (p.Gly128Glu)	not specified [RCV004196481]	uncertain significance	1	13513211	13513211	Human		name
156188451	CV2342217	single nucleotide variant	NM_001172779.2(LRRC34):c.821G>T (p.Cys274Phe)	not specified [RCV004191798]	uncertain significance	3	169796832	169796832	Human		name
155980262	CV2343455	single nucleotide variant	NM_014834.4(LRRC37A):c.4241C>A (p.Ser1414Tyr)	not specified [RCV004197527]	uncertain significance	17	46331518	46331518	Human		name
156342784	CV2344097	single nucleotide variant	NM_001172779.2(LRRC34):c.365G>A (p.Cys122Tyr)	not specified [RCV004195701]	uncertain significance	3	169807602	169807602	Human		name
155907122	CV2354368	single nucleotide variant	NM_001128922.2(LRRC32):c.427C>T (p.Arg143Trp)	not specified [RCV004200322]	uncertain significance	11	76661166	76661166	Human		name
155924899	CV2358231	single nucleotide variant	NM_014834.4(LRRC37A):c.4235C>T (p.Thr1412Ile)	not specified [RCV004212023]	uncertain significance	17	46331512	46331512	Human		name
156144215	CV2358646	single nucleotide variant	NM_014834.4(LRRC37A):c.4322C>G (p.Thr1441Ser)	not specified [RCV004207519]	uncertain significance	17	46331599	46331599	Human		name
156051429	CV2363164	single nucleotide variant	NM_001105581.3(LRRC30):c.860G>T (p.Gly287Val)	not specified [RCV004213734]	uncertain significance	18	7231998	7231998	Human		name
156077397	CV2375100	single nucleotide variant	NM_001195545.2(LRRC3C):c.361G>T (p.Ala121Ser)	not specified [RCV004230145]	uncertain significance	17	39944267	39944267	Human		name
155937075	CV2379955	single nucleotide variant	NM_014834.4(LRRC37A):c.4882T>C (p.Trp1628Arg)	not specified [RCV004222099]	uncertain significance	17	46337318	46337318	Human		name
156145046	CV2383974	single nucleotide variant	NM_001195545.2(LRRC3C):c.641G>T (p.Trp214Leu)	not specified [RCV004224951]	uncertain significance	17	39944547	39944547	Human		name
156043614	CV2388000	single nucleotide variant	NM_199340.5(LRRC37A3):c.1760G>A (p.Gly587Glu)	not specified [RCV004236533]	likely benign	17	64895498	64895498	Human		name
156164799	CV2389736	single nucleotide variant	NM_199340.5(LRRC37A3):c.2335C>T (p.Arg779Trp)	not specified [RCV004243782]	uncertain significance	17	64894923	64894923	Human		name
155959207	CV2390499	single nucleotide variant	NM_199340.5(LRRC37A3):c.1736T>C (p.Val579Ala)	not specified [RCV004239036]	likely benign	17	64895522	64895522	Human		name
156051883	CV2391278	single nucleotide variant	NM_199340.5(LRRC37A3):c.1936C>T (p.Pro646Ser)	not specified [RCV004237283]	uncertain significance	17	64895322	64895322	Human		name
156258229	CV2395342	single nucleotide variant	NM_199340.5(LRRC37A3):c.1780G>C (p.Gly594Arg)	not specified [RCV004239434]	uncertain significance	17	64895478	64895478	Human		name
156261174	CV2395604	single nucleotide variant	NM_199340.5(LRRC37A3):c.1321C>T (p.Arg441Trp)	not specified [RCV004241453]	uncertain significance	17	64895937	64895937	Human		name
156104582	CV2400302	single nucleotide variant	NM_199340.5(LRRC37A3):c.2260G>A (p.Ala754Thr)	not specified [RCV004244362]	likely benign	17	64894998	64894998	Human		name
156105491	CV2400374	single nucleotide variant	NM_199340.5(LRRC37A3):c.2915A>G (p.Asn972Ser)	not specified [RCV004244426]	likely benign	17	64869158	64869158	Human		name
156226077	CV2401052	single nucleotide variant	NM_014834.4(LRRC37A):c.4483G>T (p.Ala1495Ser)	not specified [RCV004244325]	likely benign	17	46331760	46331760	Human		name
156005809	CV2401132	single nucleotide variant	NM_199340.5(LRRC37A3):c.1816G>A (p.Val606Ile)	not specified [RCV004245697]	uncertain significance	17	64895442	64895442	Human		name
329367809	CV2427570	single nucleotide variant	NM_001010847.2(LRRC38):c.685C>T (p.Arg229Cys)	not specified [RCV004250206]	uncertain significance	1	13476046	13476046	Human		name
329350208	CV2442591	single nucleotide variant	NM_014834.4(LRRC37A):c.3557G>A (p.Ser1186Asn)	not specified [RCV004264952]	uncertain significance	17	46330834	46330834	Human		name
329380296	CV2444307	single nucleotide variant	NM_199340.5(LRRC37A3):c.2321C>T (p.Ala774Val)	not specified [RCV004263067]	uncertain significance	17	64894937	64894937	Human		name
329350051	CV2445476	single nucleotide variant	NM_014834.4(LRRC37A):c.3604G>A (p.Glu1202Lys)	not specified [RCV004257535]	likely benign	17	46330881	46330881	Human		name
329349911	CV2456200	single nucleotide variant	NM_014834.4(LRRC37A):c.4100C>A (p.Pro1367His)	not specified [RCV004273386]	uncertain significance	17	46331377	46331377	Human		name
329397521	CV2456260	single nucleotide variant	NM_001195545.2(LRRC3C):c.688G>A (p.Gly230Arg)	not specified [RCV004275437]	uncertain significance	17	39944594	39944594	Human		name
329350070	CV2457523	single nucleotide variant	NM_001006607.3(LRRC37A2):c.97C>G (p.Leu33Val)	not specified [RCV004267332]	uncertain significance	17	46512809	46512809	Human		name
401735806	CV2672746	single nucleotide variant	NM_001105581.3(LRRC30):c.544G>C (p.Val182Leu)	not specified [RCV004287758]	uncertain significance	18	7231682	7231682	Human		name
401720137	CV2675785	single nucleotide variant	NM_001195545.2(LRRC3C):c.362C>T (p.Ala121Val)	not specified [RCV004288026]	uncertain significance	17	39944268	39944268	Human		name
401722767	CV2677096	single nucleotide variant	NM_001010847.2(LRRC38):c.452T>C (p.Leu151Pro)	not specified [RCV004295733]	uncertain significance	1	13513142	13513142	Human		name
401782470	CV2686876	single nucleotide variant	NM_001105581.3(LRRC30):c.611G>A (p.Ser204Asn)	not specified [RCV004302053]	uncertain significance	18	7231749	7231749	Human		name
401756508	CV2687184	single nucleotide variant	NM_199340.5(LRRC37A3):c.1777C>G (p.Pro593Ala)	not specified [RCV004298133]	uncertain significance	17	64895481	64895481	Human		name
401747705	CV2691218	single nucleotide variant	NM_014834.4(LRRC37A):c.3484C>G (p.Gln1162Glu)	not specified [RCV004302991]	uncertain significance	17	46330761	46330761	Human		name
401745751	CV2693342	single nucleotide variant	NM_001010847.2(LRRC38):c.320T>C (p.Val107Ala)	not specified [RCV004295305]	likely benign	1	13513274	13513274	Human		name
401761874	CV2699441	single nucleotide variant	NM_199340.5(LRRC37A3):c.1109C>T (p.Ser370Phe)	not specified [RCV004299665]	uncertain significance	17	64896149	64896149	Human		name
401751046	CV2700156	single nucleotide variant	NM_001010847.2(LRRC38):c.503G>A (p.Ser168Asn)	not specified [RCV004310553]	likely benign	1	13513091	13513091	Human		name
401751050	CV2700158	single nucleotide variant	NM_001010847.2(LRRC38):c.538T>A (p.Ser180Thr)	not specified [RCV004310555]	likely benign	1	13513056	13513056	Human		name
401720630	CV2702005	single nucleotide variant	NM_199340.5(LRRC37A3):c.2044C>G (p.Pro682Ala)	not specified [RCV004320595]	uncertain significance	17	64895214	64895214	Human		name
401722498	CV2703393	single nucleotide variant	NM_199340.5(LRRC37A3):c.2218A>G (p.Thr740Ala)	not specified [RCV004315735]	uncertain significance	17	64895040	64895040	Human		name
401763407	CV2703821	single nucleotide variant	NM_199340.5(LRRC37A3):c.1962G>T (p.Gln654His)	not specified [RCV004306689]	uncertain significance	17	64895296	64895296	Human		name
401748447	CV2705018	single nucleotide variant	NM_001128922.2(LRRC32):c.542A>G (p.His181Arg)	not specified [RCV004309940]	uncertain significance	11	76661051	76661051	Human		name
401738268	CV2711742	single nucleotide variant	NM_001195545.2(LRRC3C):c.747T>G (p.Asp249Glu)	not specified [RCV004309399]	uncertain significance	17	39944653	39944653	Human		name
401745472	CV2713558	single nucleotide variant	NM_014834.4(LRRC37A):c.3023T>A (p.Ile1008Asn)	not specified [RCV004320939]	uncertain significance	17	46322997	46322997	Human		name
401743072	CV2715388	single nucleotide variant	NM_001321350.2(LRRC37B):c.164T>A (p.Leu55His)	not specified [RCV004324710]	uncertain significance	17	32021556	32021556	Human		name
401768800	CV2716734	single nucleotide variant	NM_199340.5(LRRC37A3):c.2965G>A (p.Ala989Thr)	not specified [RCV004327778]	uncertain significance	17	64869108	64869108	Human		name
401746406	CV2717916	single nucleotide variant	NM_014834.4(LRRC37A):c.4562C>T (p.Thr1521Ile)	not specified [RCV004321879]	uncertain significance	17	46331839	46331839	Human		name
401761959	CV2726976	single nucleotide variant	NM_001321350.2(LRRC37B):c.193G>A (p.Val65Ile)	not specified [RCV004325044]	uncertain significance	17	32021585	32021585	Human		name
401767867	CV2729975	single nucleotide variant	NM_001010847.2(LRRC38):c.437A>C (p.Asp146Ala)	not specified [RCV004332966]	likely benign	1	13513157	13513157	Human		name
401860750	CV2758606	single nucleotide variant	NM_001128922.2(LRRC32):c.334G>A (p.Ala112Thr)	not specified [RCV004337687]	uncertain significance	11	76661259	76661259	Human		name
401879180	CV2764884	single nucleotide variant	NM_001172779.2(LRRC34):c.395A>G (p.Tyr132Cys)	not specified [RCV004334977]	uncertain significance	3	169807475	169807475	Human		name
401863117	CV2765532	single nucleotide variant	NM_001105581.3(LRRC30):c.422A>G (p.Lys141Arg)	not specified [RCV004342236]	uncertain significance	18	7231560	7231560	Human		name
401876455	CV2770908	single nucleotide variant	NM_001105581.3(LRRC30):c.307G>C (p.Gly103Arg)	not specified [RCV004343580]	uncertain significance	18	7231445	7231445	Human		name
401887495	CV2771972	single nucleotide variant	NM_001105581.3(LRRC30):c.383G>T (p.Cys128Phe)	not specified [RCV004344661]	uncertain significance	18	7231521	7231521	Human		name
401884818	CV2774593	single nucleotide variant	NM_199340.5(LRRC37A3):c.1039C>T (p.Pro347Ser)	not specified [RCV004350067]	uncertain significance	17	64896219	64896219	Human		name
401864489	CV2777860	single nucleotide variant	NM_199340.5(LRRC37A3):c.2374G>C (p.Gly792Arg)	not specified [RCV004346045]	uncertain significance	17	64894884	64894884	Human		name
401896394	CV2781237	single nucleotide variant	NM_001128922.2(LRRC32):c.655C>G (p.Gln219Glu)	not specified [RCV004352273]	uncertain significance	11	76660938	76660938	Human		name
401898357	CV2787721	single nucleotide variant	NM_001172779.2(LRRC34):c.298C>A (p.Arg100Ser)	not specified [RCV004356638]	uncertain significance	3	169807669	169807669	Human		name
401903891	CV2811234	single nucleotide variant	NM_001321350.2(LRRC37B):c.1737C>G (p.Leu579=)	not provided [RCV003419706]	likely benign	17	32034916	32034916	Human		name
401929091	CV2813558	single nucleotide variant	NM_001128922.2(LRRC32):c.592C>T (p.Arg198Cys)	not provided [RCV003390094]	likely benign	11	76661001	76661001	Human		name
405655499	CV3277251	single nucleotide variant	NM_001105581.3(LRRC30):c.526G>T (p.Ala176Ser)	not specified [RCV004415404]	uncertain significance	18	7231664	7231664	Human		name
405655503	CV3277253	single nucleotide variant	NM_001105581.3(LRRC30):c.805C>T (p.Leu269Phe)	not specified [RCV004415406]	uncertain significance	18	7231943	7231943	Human		name
405655505	CV3277254	single nucleotide variant	NM_001105581.3(LRRC30):c.899A>T (p.His300Leu)	not specified [RCV004415407]	uncertain significance	18	7232037	7232037	Human		name
405655558	CV3277278	single nucleotide variant	NM_001128922.2(LRRC32):c.322C>T (p.Arg108Trp)	not specified [RCV004415431]	uncertain significance	11	76661271	76661271	Human		name
405655560	CV3277279	single nucleotide variant	NM_001128922.2(LRRC32):c.376G>A (p.Val126Met)	not specified [RCV004415432]	uncertain significance	11	76661217	76661217	Human		name
405655562	CV3277280	single nucleotide variant	NM_001128922.2(LRRC32):c.404G>A (p.Ser135Asn)	not specified [RCV004415433]	uncertain significance	11	76661189	76661189	Human		name
405655563	CV3277281	single nucleotide variant	NM_001128922.2(LRRC32):c.496C>T (p.Arg166Cys)	not specified [RCV004415434]	uncertain significance	11	76661097	76661097	Human		name
405655565	CV3277282	single nucleotide variant	NM_001128922.2(LRRC32):c.570T>A (p.Asp190Glu)	not specified [RCV004415435]	uncertain significance	11	76661023	76661023	Human		name
405655567	CV3277283	single nucleotide variant	NM_001128922.2(LRRC32):c.751C>T (p.Arg251Trp)	not specified [RCV004415436]	uncertain significance	11	76660842	76660842	Human		name
405655568	CV3277284	single nucleotide variant	NM_001128922.2(LRRC32):c.931G>A (p.Gly311Ser)	not specified [RCV004415437]	uncertain significance	11	76660662	76660662	Human		name
405655569	CV3277285	single nucleotide variant	NM_001128922.2(LRRC32):c.998G>A (p.Ser333Asn)	not specified [RCV004415438]	uncertain significance	11	76660595	76660595	Human		name
405655575	CV3277288	single nucleotide variant	NM_001172779.2(LRRC34):c.535C>T (p.Arg179Trp)	not specified [RCV004415441]	uncertain significance	3	169804175	169804175	Human		name
405655576	CV3277289	single nucleotide variant	NM_001172779.2(LRRC34):c.646G>A (p.Asp216Asn)	not specified [RCV004415442]	uncertain significance	3	169804064	169804064	Human		name
405655578	CV3277290	single nucleotide variant	NM_001172779.2(LRRC34):c.778C>T (p.Arg260Cys)	not specified [RCV004415443]	uncertain significance	3	169796875	169796875	Human		name
405655579	CV3277291	single nucleotide variant	NM_001172779.2(LRRC34):c.809C>T (p.Ala270Val)	not specified [RCV004415444]	likely benign	3	169796844	169796844	Human		name
405655581	CV3277292	single nucleotide variant	NM_001172779.2(LRRC34):c.859T>C (p.Cys287Arg)	not specified [RCV004415445]	uncertain significance	3	169796794	169796794	Human		name
405655611	CV3277308	single nucleotide variant	NM_014834.4(LRRC37A):c.3730G>A (p.Ala1244Thr)	not specified [RCV004415461]	uncertain significance	17	46331007	46331007	Human		name
405655613	CV3277309	single nucleotide variant	NM_014834.4(LRRC37A):c.3890C>G (p.Pro1297Arg)	not specified [RCV004415462]	uncertain significance	17	46331167	46331167	Human		name
405655615	CV3277310	single nucleotide variant	NM_014834.4(LRRC37A):c.4001G>A (p.Ser1334Asn)	not specified [RCV004415463]	uncertain significance	17	46331278	46331278	Human		name
405655618	CV3277311	single nucleotide variant	NM_014834.4(LRRC37A):c.4282G>T (p.Ala1428Ser)	not specified [RCV004415464]	uncertain significance	17	46331559	46331559	Human		name
405655621	CV3277312	single nucleotide variant	NM_014834.4(LRRC37A):c.4400C>T (p.Ser1467Leu)	not specified [RCV004415465]	uncertain significance	17	46331677	46331677	Human		name
405655623	CV3277313	single nucleotide variant	NM_014834.4(LRRC37A):c.4612A>G (p.Lys1538Glu)	not specified [RCV004415466]	likely benign	17	46331889	46331889	Human		name
405655626	CV3277314	single nucleotide variant	NM_014834.4(LRRC37A):c.4791A>G (p.Ile1597Met)	not specified [RCV004415467]	uncertain significance	17	46332638	46332638	Human		name
405655629	CV3277315	single nucleotide variant	NM_014834.4(LRRC37A):c.5072C>T (p.Thr1691Met)	not specified [RCV004415468]	uncertain significance	17	46337692	46337692	Human		name
405655637	CV3277318	single nucleotide variant	NM_001006607.3(LRRC37A2):c.29T>C (p.Val10Ala)	not specified [RCV004415471]	likely benign	17	46512741	46512741	Human		name
405655687	CV3277336	single nucleotide variant	NM_001006607.3(LRRC37A2):c.50G>A (p.Arg17His)	not specified [RCV004415489]	uncertain significance	17	46512762	46512762	Human		name
405655695	CV3277339	single nucleotide variant	NM_199340.5(LRRC37A3):c.1190C>G (p.Pro397Arg)	not specified [RCV004415492]	uncertain significance	17	64896068	64896068	Human		name
405655697	CV3277340	single nucleotide variant	NM_199340.5(LRRC37A3):c.1258A>G (p.Thr420Ala)	not specified [RCV004415493]	uncertain significance	17	64896000	64896000	Human		name
405655702	CV3277342	single nucleotide variant	NM_199340.5(LRRC37A3):c.1853C>T (p.Thr618Ile)	not specified [RCV004415495]	uncertain significance	17	64895405	64895405	Human		name
405655761	CV3277376	single nucleotide variant	NM_001321350.2(LRRC37B):c.101C>A (p.Ala34Asp)	not specified [RCV004415529]	uncertain significance	17	32021493	32021493	Human		name
405655763	CV3277377	single nucleotide variant	NM_001321350.2(LRRC37B):c.206G>A (p.Arg69His)	not specified [RCV004415530]	uncertain significance	17	32021598	32021598	Human		name
405655764	CV3277378	single nucleotide variant	NM_001321350.2(LRRC37B):c.229G>C (p.Asp77His)	not specified [RCV004415531]	uncertain significance	17	32021621	32021621	Human		name
405655776	CV3277385	single nucleotide variant	NM_001010847.2(LRRC38):c.671G>A (p.Arg224Lys)	not specified [RCV004415538]	uncertain significance	1	13476060	13476060	Human		name
405655778	CV3277386	single nucleotide variant	NM_001010847.2(LRRC38):c.772G>A (p.Val258Met)	not specified [RCV004415539]	uncertain significance	1	13475959	13475959	Human		name
405655779	CV3277387	single nucleotide variant	NM_001010847.2(LRRC38):c.854C>T (p.Ala285Val)	not specified [RCV004415540]	uncertain significance	1	13475877	13475877	Human		name
405655800	CV3277400	single nucleotide variant	NM_001195545.2(LRRC3C):c.371A>T (p.Gln124Leu)	not specified [RCV004415553]	uncertain significance	17	39944277	39944277	Human		name
405655802	CV3277401	single nucleotide variant	NM_001195545.2(LRRC3C):c.575G>A (p.Arg192Gln)	not specified [RCV004415554]	uncertain significance	17	39944481	39944481	Human		name
405655804	CV3277402	single nucleotide variant	NM_001195545.2(LRRC3C):c.575G>T (p.Arg192Leu)	not specified [RCV004415555]	uncertain significance	17	39944481	39944481	Human		name
407500697	CV3456427	single nucleotide variant	NM_001105581.3(LRRC30):c.554T>C (p.Leu185Pro)	not specified [RCV004644675]	uncertain significance	18	7231692	7231692	Human		name
407500703	CV3456429	single nucleotide variant	NM_001105581.3(LRRC30):c.726T>G (p.Asn242Lys)	not specified [RCV004644677]	uncertain significance	18	7231864	7231864	Human		name
407500708	CV3456430	single nucleotide variant	NM_001105581.3(LRRC30):c.434T>C (p.Leu145Pro)	not specified [RCV004644678]	uncertain significance	18	7231572	7231572	Human		name
407500712	CV3456431	single nucleotide variant	NM_001105581.3(LRRC30):c.533T>C (p.Ile178Thr)	not specified [RCV004644679]	uncertain significance	18	7231671	7231671	Human		name
407468121	CV3456434	single nucleotide variant	NM_001128922.2(LRRC32):c.778G>A (p.Asp260Asn)	not specified [RCV004636161]	uncertain significance	11	76660815	76660815	Human		name
407500725	CV3456435	single nucleotide variant	NM_001128922.2(LRRC32):c.511G>A (p.Asp171Asn)	not specified [RCV004644682]	uncertain significance	11	76661082	76661082	Human		name
407500730	CV3456436	single nucleotide variant	NM_001128922.2(LRRC32):c.508C>T (p.Arg170Trp)	not specified [RCV004644683]	likely benign	11	76661085	76661085	Human		name
407500749	CV3456440	single nucleotide variant	NM_001128922.2(LRRC32):c.944C>G (p.Ser315Cys)	not specified [RCV004644687]	uncertain significance	11	76660649	76660649	Human		name
407468128	CV3456442	single nucleotide variant	NM_001128922.2(LRRC32):c.731A>G (p.Gln244Arg)	not specified [RCV004636163]	uncertain significance	11	76660862	76660862	Human		name
407500764	CV3456446	single nucleotide variant	NM_001128922.2(LRRC32):c.873C>A (p.His291Gln)	not specified [RCV004644690]	uncertain significance	11	76660720	76660720	Human		name
407481595	CV3456455	single nucleotide variant	NM_014834.4(LRRC37A):c.4817G>A (p.Cys1606Tyr)	not specified [RCV004644695]	uncertain significance	17	46335552	46335552	Human		name
407481600	CV3456456	single nucleotide variant	NM_014834.4(LRRC37A):c.4936C>G (p.Gln1646Glu)	not specified [RCV004644696]	uncertain significance	17	46337450	46337450	Human		name
407485478	CV3456457	single nucleotide variant	NM_014834.4(LRRC37A):c.3691G>A (p.Val1231Ile)	not specified [RCV004644697]	uncertain significance	17	46330968	46330968	Human		name
407485166	CV3456462	single nucleotide variant	NM_014834.4(LRRC37A):c.4778C>T (p.Thr1593Met)	not specified [RCV004644700]	likely benign	17	46332625	46332625	Human		name
407485171	CV3456463	single nucleotide variant	NM_014834.4(LRRC37A):c.4221C>A (p.Asn1407Lys)	not specified [RCV004644701]	uncertain significance	17	46331498	46331498	Human		name
407500804	CV3456474	single nucleotide variant	NM_199340.5(LRRC37A3):c.2381C>G (p.Pro794Arg)	not specified [RCV004644710]	uncertain significance	17	64894877	64894877	Human		name
407500820	CV3456477	single nucleotide variant	NM_199340.5(LRRC37A3):c.1151G>A (p.Gly384Asp)	not specified [RCV004644713]	uncertain significance	17	64896107	64896107	Human		name
407500826	CV3456479	single nucleotide variant	NM_199340.5(LRRC37A3):c.2134C>T (p.His712Tyr)	not specified [RCV004644715]	uncertain significance	17	64895124	64895124	Human		name
407500835	CV3456482	single nucleotide variant	NM_001321350.2(LRRC37B):c.278T>C (p.Leu93Pro)	not specified [RCV004644717]	uncertain significance	17	32021670	32021670	Human		name
407500844	CV3456484	single nucleotide variant	NM_001321350.2(LRRC37B):c.142A>G (p.Arg48Gly)	not specified [RCV004644719]	uncertain significance	17	32021534	32021534	Human		name
407500866	CV3456491	single nucleotide variant	NM_001010847.2(LRRC38):c.754A>G (p.Ile252Val)	not specified [RCV004644725]	uncertain significance	1	13475977	13475977	Human		name
407468160	CV3456492	single nucleotide variant	NM_001010847.2(LRRC38):c.326T>A (p.Leu109His)	not specified [RCV004636175]	uncertain significance	1	13513268	13513268	Human		name
407500899	CV3456501	single nucleotide variant	NM_001195545.2(LRRC3C):c.433G>A (p.Val145Met)	not specified [RCV004644734]	uncertain significance	17	39944339	39944339	Human		name
407500905	CV3456502	single nucleotide variant	NM_001195545.2(LRRC3C):c.523G>C (p.Val175Leu)	not specified [RCV004644735]	uncertain significance	17	39944429	39944429	Human		name
597626195	CV3693396	single nucleotide variant	NM_001195545.2(LRRC3C):c.499G>A (p.Ala167Thr)	not specified [RCV004938558]	uncertain significance	17	39944405	39944405	Human		name
597625945	CV3696781	single nucleotide variant	NM_001105581.3(LRRC30):c.763T>A (p.Cys255Ser)	not specified [RCV004938469]	uncertain significance	18	7231901	7231901	Human		name
597625948	CV3696782	single nucleotide variant	NM_001105581.3(LRRC30):c.472T>C (p.Cys158Arg)	not specified [RCV004938470]	uncertain significance	18	7231610	7231610	Human		name
597625982	CV3696795	single nucleotide variant	NM_001128922.2(LRRC32):c.829A>C (p.Ile277Leu)	not specified [RCV004938480]	uncertain significance	11	76660764	76660764	Human		name
597626174	CV3696796	single nucleotide variant	NM_001128922.2(LRRC32):c.787G>A (p.Ala263Thr)	not specified [RCV004938481]	uncertain significance	11	76660806	76660806	Human		name
597626163	CV3696801	single nucleotide variant	NM_001128922.2(LRRC32):c.925G>A (p.Ala309Thr)	not specified [RCV004938484]	uncertain significance	11	76660668	76660668	Human		name
597626154	CV3696805	single nucleotide variant	NM_001128922.2(LRRC32):c.625C>T (p.Leu209Phe)	not specified [RCV004938487]	uncertain significance	11	76660968	76660968	Human		name
597626147	CV3696807	single nucleotide variant	NM_001172779.2(LRRC34):c.674T>C (p.Ile225Thr)	not specified [RCV004938489]	uncertain significance	3	169800738	169800738	Human		name
597626145	CV3696809	single nucleotide variant	NM_001172779.2(LRRC34):c.736A>C (p.Ile246Leu)	not specified [RCV004938490]	uncertain significance	3	169800676	169800676	Human		name
597626141	CV3696810	single nucleotide variant	NM_001172779.2(LRRC34):c.514G>A (p.Ala172Thr)	not specified [RCV004938491]	uncertain significance	3	169806862	169806862	Human		name
597626138	CV3696812	single nucleotide variant	NM_001172779.2(LRRC34):c.779G>A (p.Arg260His)	not specified [RCV004938492]	likely benign	3	169796874	169796874	Human		name
597697477	CV3696825	single nucleotide variant	NM_014834.4(LRRC37A):c.3670G>A (p.Glu1224Lys)	not specified [RCV004938502]	uncertain significance	17	46330947	46330947	Human		name
597697465	CV3696826	single nucleotide variant	NM_014834.4(LRRC37A):c.3450C>A (p.Ser1150Arg)	not specified [RCV004938503]	uncertain significance	17	46330727	46330727	Human		name
597697446	CV3696828	single nucleotide variant	NM_014834.4(LRRC37A):c.4492A>G (p.Ile1498Val)	not specified [RCV004938505]	uncertain significance	17	46331769	46331769	Human		name
597697435	CV3696829	single nucleotide variant	NM_014834.4(LRRC37A):c.3566G>A (p.Arg1189Lys)	not specified [RCV004938506]	uncertain significance	17	46330843	46330843	Human		name
597625998	CV3696854	single nucleotide variant	NM_199340.5(LRRC37A3):c.1297C>G (p.Leu433Val)	not specified [RCV004938524]	uncertain significance	17	64895961	64895961	Human		name
597626001	CV3696855	single nucleotide variant	NM_199340.5(LRRC37A3):c.2096C>A (p.Thr699Lys)	not specified [RCV004938525]	uncertain significance	17	64895162	64895162	Human		name
597626011	CV3696858	single nucleotide variant	NM_199340.5(LRRC37A3):c.2383A>G (p.Thr795Ala)	not specified [RCV004938528]	uncertain significance	17	64894875	64894875	Human		name
597626014	CV3696861	single nucleotide variant	NM_199340.5(LRRC37A3):c.1066T>G (p.Ser356Ala)	not specified [RCV004938529]	uncertain significance	17	64896192	64896192	Human		name
597626018	CV3696862	single nucleotide variant	NM_199340.5(LRRC37A3):c.1739C>G (p.Pro580Arg)	not specified [RCV004938530]	uncertain significance	17	64895519	64895519	Human		name
597626024	CV3696864	single nucleotide variant	NM_199340.5(LRRC37A3):c.2195C>T (p.Thr732Ile)	not specified [RCV004938532]	uncertain significance	17	64895063	64895063	Human		name
597626034	CV3696868	single nucleotide variant	NM_199340.5(LRRC37A3):c.2248G>A (p.Asp750Asn)	not specified [RCV004938535]	uncertain significance	17	64895010	64895010	Human		name
597626044	CV3696872	single nucleotide variant	NM_001321350.2(LRRC37B):c.254A>G (p.Gln85Arg)	not specified [RCV004938538]	uncertain significance	17	32021646	32021646	Human		name
597626061	CV3696880	single nucleotide variant	NM_001321350.2(LRRC37B):c.144G>C (p.Arg48Ser)	not specified [RCV004938543]	uncertain significance	17	32021536	32021536	Human		name
597626068	CV3696885	single nucleotide variant	NM_001321350.2(LRRC37B):c.250C>T (p.His84Tyr)	not specified [RCV004938545]	uncertain significance	17	32021642	32021642	Human		name
597626072	CV3696886	single nucleotide variant	NM_001010847.2(LRRC38):c.782C>T (p.Ala261Val)	not specified [RCV004938546]	uncertain significance	1	13475949	13475949	Human		name
597626075	CV3696887	single nucleotide variant	NM_001010847.2(LRRC38):c.520G>T (p.Ala174Ser)	not specified [RCV004938547]	uncertain significance	1	13513074	13513074	Human		name
597626079	CV3696888	single nucleotide variant	NM_001010847.2(LRRC38):c.573C>G (p.Asp191Glu)	not specified [RCV004938548]	uncertain significance	1	13513021	13513021	Human		name
598273053	CV3984677	single nucleotide variant	NM_001321350.2(LRRC37B):c.148C>T (p.Pro50Ser)	not specified [RCV005350620]	uncertain significance	17	32021540	32021540	Human		name
598250990	CV3984679	single nucleotide variant	NM_001010847.2(LRRC38):c.431A>G (p.His144Arg)	not specified [RCV005366604]	uncertain significance	1	13513163	13513163	Human		name
598273062	CV3984681	single nucleotide variant	NM_001010847.2(LRRC38):c.861T>A (p.Asp287Glu)	not specified [RCV005350622]	uncertain significance	1	13475870	13475870	Human		name
598273066	CV3984682	single nucleotide variant	NM_001010847.2(LRRC38):c.373C>T (p.Arg125Cys)	not specified [RCV005350623]	uncertain significance	1	13513221	13513221	Human		name
598222309	CV3984688	single nucleotide variant	NM_001195545.2(LRRC3C):c.653G>A (p.Arg218Gln)	not specified [RCV005379872]	likely benign	17	39944559	39944559	Human		name
598251014	CV3984690	single nucleotide variant	NM_001195545.2(LRRC3C):c.380A>G (p.Glu127Gly)	not specified [RCV005366608]	uncertain significance	17	39944286	39944286	Human		name
598272869	CV3988263	single nucleotide variant	NM_001105581.3(LRRC30):c.782C>T (p.Ala261Val)	not specified [RCV005350582]	uncertain significance	18	7231920	7231920	Human		name
598250794	CV3988269	single nucleotide variant	NM_001128922.2(LRRC32):c.323G>A (p.Arg108Gln)	not specified [RCV005366572]	uncertain significance	11	76661270	76661270	Human		name
598250800	CV3988270	single nucleotide variant	NM_001128922.2(LRRC32):c.488G>A (p.Arg163His)	not specified [RCV005366573]	uncertain significance	11	76661105	76661105	Human		name
598250812	CV3988274	single nucleotide variant	NM_001128922.2(LRRC32):c.436G>A (p.Gly146Arg)	not specified [RCV005366575]	uncertain significance	11	76661157	76661157	Human		name
598272894	CV3988275	single nucleotide variant	NM_001128922.2(LRRC32):c.976G>C (p.Glu326Gln)	not specified [RCV005350587]	uncertain significance	11	76660617	76660617	Human		name
598272900	CV3988276	single nucleotide variant	NM_001128922.2(LRRC32):c.940C>G (p.Leu314Val)	not specified [RCV005350588]	uncertain significance	11	76660653	76660653	Human		name
598272904	CV3988277	single nucleotide variant	NM_001128922.2(LRRC32):c.598A>G (p.Thr200Ala)	not specified [RCV005350589]	likely benign	11	76660995	76660995	Human		name
598272909	CV3988278	single nucleotide variant	NM_001172779.2(LRRC34):c.917T>C (p.Ile306Thr)	not specified [RCV005350590]	uncertain significance	3	169796361	169796361	Human		name
598250819	CV3988280	single nucleotide variant	NM_001172779.2(LRRC34):c.382T>A (p.Leu128Met)	not specified [RCV005366576]	uncertain significance	3	169807488	169807488	Human		name
598272914	CV3988281	single nucleotide variant	NM_001172779.2(LRRC34):c.511A>G (p.Ile171Val)	not specified [RCV005350591]	uncertain significance	3	169806865	169806865	Human		name
598250863	CV3988297	single nucleotide variant	NM_014834.4(LRRC37A):c.3922C>T (p.His1308Tyr)	not specified [RCV005366584]	uncertain significance	17	46331199	46331199	Human		name
598231555	CV3988313	single nucleotide variant	NM_199340.5(LRRC37A3):c.1193G>T (p.Gly398Val)	not specified [RCV005362884]	uncertain significance	17	64896065	64896065	Human		name
598272984	CV3988314	single nucleotide variant	NM_199340.5(LRRC37A3):c.1249G>A (p.Val417Met)	not specified [RCV005350604]	uncertain significance	17	64896009	64896009	Human		name
598272999	CV3988319	single nucleotide variant	NM_199340.5(LRRC37A3):c.1187C>T (p.Pro396Leu)	not specified [RCV005350607]	uncertain significance	17	64896071	64896071	Human		name
598250935	CV3988320	single nucleotide variant	NM_199340.5(LRRC37A3):c.1721C>T (p.Pro574Leu)	not specified [RCV005366595]	uncertain significance	17	64895537	64895537	Human		name
15177642	CV713189	single nucleotide variant	NM_001128922.2(LRRC32):c.374G>A (p.Arg125His)	not provided [RCV000973478]	benign	11	76661219	76661219	Human		name
8636297	CV91520	single nucleotide variant	NM_199340.3(LRRC37A3):c.2978T>G (p.Leu993Arg)	Malignant melanoma [RCV000071618]	not provided	17	64869095	64869095	Human		name
8636298	CV91521	single nucleotide variant	NM_199340.3(LRRC37A3):c.1129C>T (p.Pro377Ser)	Malignant melanoma [RCV000071619]	not provided	17	64896129	64896129	Human		name
156319952	CV2197191	single nucleotide variant	NM_001128922.2(LRRC32):c.1567G>A (p.Glu523Lys)	not specified [RCV004078981]	uncertain significance	11	76660026	76660026	Human		name
156140322	CV2202970	single nucleotide variant	NM_001128922.2(LRRC32):c.1448C>T (p.Thr483Met)	not specified [RCV004069232]	uncertain significance	11	76660145	76660145	Human		name
156247975	CV2203015	single nucleotide variant	NM_001128922.2(LRRC32):c.1559A>G (p.Asn520Ser)	not specified [RCV004069269]	uncertain significance	11	76660034	76660034	Human		name
156261883	CV2204941	single nucleotide variant	NM_199340.5(LRRC37A3):c.3230G>A (p.Arg1077Gln)	not specified [RCV004075181]	uncertain significance	17	64860916	64860916	Human		name
156244107	CV2207198	single nucleotide variant	NM_199340.5(LRRC37A3):c.4565G>A (p.Gly1522Asp)	not specified [RCV004087930]	uncertain significance	17	64859581	64859581	Human		name
156110548	CV2207655	single nucleotide variant	NM_001128922.2(LRRC32):c.1504G>A (p.Gly502Arg)	not specified [RCV004090428]	uncertain significance	11	76660089	76660089	Human		name
156152217	CV2209342	single nucleotide variant	NM_199340.5(LRRC37A3):c.4624G>T (p.Asp1542Tyr)	not specified [RCV004093519]	uncertain significance	17	64859522	64859522	Human		name
156387506	CV2221528	single nucleotide variant	NM_001128922.2(LRRC32):c.1472C>T (p.Ala491Val)	not specified [RCV004096796]	uncertain significance	11	76660121	76660121	Human		name
156113039	CV2228616	single nucleotide variant	NM_199340.5(LRRC37A3):c.3898C>G (p.His1300Asp)	not specified [RCV004092844]	uncertain significance	17	64860248	64860248	Human		name
156344050	CV2229624	single nucleotide variant	NM_001128922.2(LRRC32):c.1555C>T (p.Leu519Phe)	not specified [RCV004103439]	uncertain significance	11	76660038	76660038	Human		name
155973238	CV2238941	single nucleotide variant	NM_199340.5(LRRC37A3):c.3721C>A (p.His1241Asn)	not specified [RCV004109841]	uncertain significance	17	64860425	64860425	Human		name
155916660	CV2239812	single nucleotide variant	NM_001128922.2(LRRC32):c.1430C>T (p.Pro477Leu)	not specified [RCV004108331]	uncertain significance	11	76660163	76660163	Human		name
156063237	CV2240133	single nucleotide variant	NM_001128922.2(LRRC32):c.1069C>T (p.Arg357Trp)	not specified [RCV004110896]	uncertain significance	11	76660524	76660524	Human		name
156284338	CV2249834	single nucleotide variant	NM_199340.5(LRRC37A3):c.4805T>C (p.Ile1602Thr)	not specified [RCV004122582]	uncertain significance	17	64858783	64858783	Human		name
156189183	CV2258474	single nucleotide variant	NM_199340.5(LRRC37A3):c.3266C>T (p.Pro1089Leu)	not specified [RCV004115663]	uncertain significance	17	64860880	64860880	Human		name
156366927	CV2269791	single nucleotide variant	NM_199340.5(LRRC37A3):c.3166C>T (p.His1056Tyr)	not specified [RCV004127034]	uncertain significance	17	64862906	64862906	Human		name
155923326	CV2280276	single nucleotide variant	NM_001321350.2(LRRC37B):c.796G>C (p.Val266Leu)	not specified [RCV004140478]	likely benign	17	32022188	32022188	Human		name
156087339	CV2295414	single nucleotide variant	NM_001321350.2(LRRC37B):c.518T>G (p.Val173Gly)	not specified [RCV004160538]	uncertain significance	17	32021910	32021910	Human		name
156089734	CV2295613	single nucleotide variant	NM_199340.5(LRRC37A3):c.3206C>T (p.Ala1069Val)	not specified [RCV004160696]	uncertain significance	17	64860940	64860940	Human		name
156062444	CV2316509	single nucleotide variant	NM_199340.5(LRRC37A3):c.4194A>C (p.Glu1398Asp)	not specified [RCV004169978]	uncertain significance	17	64859952	64859952	Human		name
156363319	CV2329818	single nucleotide variant	NM_001128922.2(LRRC32):c.1072C>T (p.Arg358Cys)	not specified [RCV004183280]	uncertain significance	11	76660521	76660521	Human		name
156288305	CV2336337	single nucleotide variant	NM_001128922.2(LRRC32):c.1195C>T (p.Arg399Trp)	not specified [RCV004192086]	uncertain significance	11	76660398	76660398	Human		name
156086300	CV2340995	single nucleotide variant	NM_001128922.2(LRRC32):c.1241G>A (p.Arg414Gln)	not specified [RCV004181487]	uncertain significance	11	76660352	76660352	Human		name
156220378	CV2345026	single nucleotide variant	NM_199340.5(LRRC37A3):c.4552G>A (p.Val1518Ile)	not specified [RCV004193311]	likely benign	17	64859594	64859594	Human		name
156134511	CV2347049	single nucleotide variant	NM_001128922.2(LRRC32):c.1514T>A (p.Val505Asp)	not specified [RCV004204533]	uncertain significance	11	76660079	76660079	Human		name
156165531	CV2348602	single nucleotide variant	NM_001128922.2(LRRC32):c.1304G>A (p.Gly435Asp)	not specified [RCV004195829]	uncertain significance	11	76660289	76660289	Human		name
156227131	CV2352810	single nucleotide variant	NM_001006607.3(LRRC37A2):c.260T>C (p.Leu87Pro)	not specified [RCV004198820]	uncertain significance	17	46512972	46512972	Human		name
156249720	CV2358958	single nucleotide variant	NM_199340.5(LRRC37A3):c.3937C>T (p.Arg1313Cys)	not specified [RCV004212288]	uncertain significance	17	64860209	64860209	Human		name
156015601	CV2360299	single nucleotide variant	NM_001321350.2(LRRC37B):c.914C>T (p.Thr305Ile)	not specified [RCV004208640]	uncertain significance	17	32022306	32022306	Human		name
155917828	CV2362423	single nucleotide variant	NM_199340.5(LRRC37A3):c.4488T>A (p.His1496Gln)	not specified [RCV004213045]	uncertain significance	17	64859658	64859658	Human		name
156073034	CV2365428	single nucleotide variant	NM_001128922.2(LRRC32):c.1976A>C (p.Gln659Pro)	not specified [RCV004209507]	uncertain significance	11	76659617	76659617	Human		name
156153124	CV2369348	single nucleotide variant	NM_199340.5(LRRC37A3):c.3764C>T (p.Ala1255Val)	not specified [RCV004208252]	uncertain significance	17	64860382	64860382	Human		name
155990085	CV2372007	single nucleotide variant	NM_199340.5(LRRC37A3):c.3352A>G (p.Ser1118Gly)	not specified [RCV004221682]	uncertain significance	17	64860794	64860794	Human		name
155990461	CV2374739	single nucleotide variant	NM_001321350.2(LRRC37B):c.889C>G (p.Pro297Ala)	not specified [RCV004225347]	uncertain significance	17	32022281	32022281	Human		name
156033748	CV2376614	single nucleotide variant	NM_001172779.2(LRRC34):c.1261G>A (p.Asp421Asn)	not specified [RCV004222818]	uncertain significance	3	169793769	169793769	Human		name
156184237	CV2377701	single nucleotide variant	NM_199340.5(LRRC37A3):c.3403A>G (p.Lys1135Glu)	not specified [RCV004228246]	likely benign	17	64860743	64860743	Human		name
156187784	CV2378103	single nucleotide variant	NM_199340.5(LRRC37A3):c.3383C>T (p.Ser1128Leu)	not specified [RCV004232659]	uncertain significance	17	64860763	64860763	Human		name
156269264	CV2379242	single nucleotide variant	NM_001128922.2(LRRC32):c.1166G>A (p.Arg389Gln)	not specified [RCV004223720]	uncertain significance	11	76660427	76660427	Human		name
156060982	CV2380186	single nucleotide variant	NM_001128922.2(LRRC32):c.1774G>A (p.Val592Met)	not specified [RCV004224553]	uncertain significance	11	76659819	76659819	Human		name
155935952	CV2380193	single nucleotide variant	NM_199340.5(LRRC37A3):c.4732T>C (p.Tyr1578His)	not specified [RCV004224560]	uncertain significance	17	64858856	64858856	Human		name
156068921	CV2381204	single nucleotide variant	NM_199340.5(LRRC37A3):c.4766C>T (p.Thr1589Ile)	not specified [RCV004227274]	uncertain significance	17	64858822	64858822	Human		name
156080382	CV2384632	single nucleotide variant	NM_001321350.2(LRRC37B):c.337G>T (p.Asp113Tyr)	not specified [RCV004232414]	uncertain significance	17	32021729	32021729	Human		name
156261598	CV2395638	single nucleotide variant	NM_199340.5(LRRC37A3):c.4333T>C (p.Trp1445Arg)	not specified [RCV004241480]	uncertain significance	17	64859813	64859813	Human		name
156004619	CV2396963	single nucleotide variant	NM_001321350.2(LRRC37B):c.917A>C (p.Asp306Ala)	not specified [RCV004234073]	likely benign	17	32022309	32022309	Human		name
156095926	CV2399020	single nucleotide variant	NM_001172779.2(LRRC34):c.1055G>A (p.Ser352Asn)	not specified [RCV004245324]	uncertain significance	3	169796223	169796223	Human		name
329368182	CV2424212	single nucleotide variant	NM_001321350.2(LRRC37B):c.773A>G (p.Lys258Arg)	not specified [RCV004250339]	uncertain significance	17	32022165	32022165	Human		name
329356879	CV2431179	single nucleotide variant	NM_199340.5(LRRC37A3):c.4208T>C (p.Met1403Thr)	not specified [RCV004250527]	uncertain significance	17	64859938	64859938	Human		name
329383925	CV2434919	single nucleotide variant	NM_001128922.2(LRRC32):c.1169C>T (p.Thr390Met)	not specified [RCV004250790]	uncertain significance	11	76660424	76660424	Human		name
329363606	CV2442338	single nucleotide variant	NM_199340.5(LRRC37A3):c.3206C>A (p.Ala1069Glu)	not specified [RCV004266600]	uncertain significance	17	64860940	64860940	Human		name
329379782	CV2443551	single nucleotide variant	NM_001321350.2(LRRC37B):c.758A>G (p.His253Arg)	not specified [RCV004262379]	uncertain significance	17	32022150	32022150	Human		name
329354516	CV2448329	single nucleotide variant	NM_001128922.2(LRRC32):c.1780G>A (p.Ala594Thr)	not specified [RCV004256617]	uncertain significance	11	76659813	76659813	Human		name
329393811	CV2449874	single nucleotide variant	NM_001128922.2(LRRC32):c.1337G>T (p.Arg446Leu)	not specified [RCV004268961]	uncertain significance	11	76660256	76660256	Human		name
329374231	CV2463451	single nucleotide variant	NM_001321350.2(LRRC37B):c.652C>A (p.Gln218Lys)	not specified [RCV004277282]	uncertain significance	17	32022044	32022044	Human		name
329388742	CV2469543	single nucleotide variant	NM_199340.5(LRRC37A3):c.4258A>G (p.Asn1420Asp)	not specified [RCV004282983]	uncertain significance	17	64859888	64859888	Human		name
329398581	CV2471199	single nucleotide variant	NM_199340.5(LRRC37A3):c.3794T>C (p.Leu1265Pro)	not specified [RCV004278442]	uncertain significance	17	64860352	64860352	Human		name
401744046	CV2673598	single nucleotide variant	NM_001006607.3(LRRC37A2):c.205C>T (p.Arg69Trp)	not specified [RCV004282334]	likely benign	17	46512917	46512917	Human		name
401770654	CV2685823	single nucleotide variant	NM_199340.5(LRRC37A3):c.3065G>A (p.Ser1022Asn)	not specified [RCV004294809]	uncertain significance	17	64863007	64863007	Human		name
401745120	CV2693184	single nucleotide variant	NM_199340.5(LRRC37A3):c.3250G>A (p.Glu1084Lys)	not specified [RCV004293115]	uncertain significance	17	64860896	64860896	Human		name
401748669	CV2694474	single nucleotide variant	NM_001128922.2(LRRC32):c.1510A>G (p.Met504Val)	not specified [RCV004304961]	uncertain significance	11	76660083	76660083	Human		name
401747639	CV2696753	single nucleotide variant	NM_199340.5(LRRC37A3):c.3616C>G (p.Leu1206Val)	not specified [RCV004290726]	uncertain significance	17	64860530	64860530	Human		name
401731465	CV2701378	single nucleotide variant	NM_001128922.2(LRRC32):c.1512G>T (p.Met504Ile)	not specified [RCV004311745]	uncertain significance	11	76660081	76660081	Human		name
401735712	CV2702852	single nucleotide variant	NM_001321350.2(LRRC37B):c.340C>G (p.Leu114Val)	not specified [RCV004321197]	uncertain significance	17	32021732	32021732	Human		name
401773682	CV2705483	single nucleotide variant	NM_001128922.2(LRRC32):c.1766G>A (p.Arg589His)	not specified [RCV004316573]	uncertain significance	11	76659827	76659827	Human		name
401721734	CV2710133	single nucleotide variant	NM_199340.5(LRRC37A3):c.4359C>G (p.Asp1453Glu)	not specified [RCV004315184]	uncertain significance	17	64859787	64859787	Human		name
401777425	CV2721716	single nucleotide variant	NM_001321350.2(LRRC37B):c.462C>G (p.Ser154Arg)	not specified [RCV004316193]	uncertain significance	17	32021854	32021854	Human		name
401781697	CV2722228	single nucleotide variant	NM_001321350.2(LRRC37B):c.859G>T (p.Ala287Ser)	not specified [RCV004328789]	uncertain significance	17	32022251	32022251	Human		name
401754475	CV2722710	single nucleotide variant	NM_001128922.2(LRRC32):c.1551G>T (p.Lys517Asn)	not specified [RCV004325148]	uncertain significance	11	76660042	76660042	Human		name
401780581	CV2727456	single nucleotide variant	NM_001128922.2(LRRC32):c.1385C>T (p.Ala462Val)	not specified [RCV004329661]	uncertain significance	11	76660208	76660208	Human		name
401856883	CV2755150	single nucleotide variant	NM_001172779.2(LRRC34):c.1259T>C (p.Val420Ala)	not specified [RCV004335299]	uncertain significance	3	169793771	169793771	Human		name
401856901	CV2755172	single nucleotide variant	NM_199340.5(LRRC37A3):c.3356C>T (p.Thr1119Ile)	not specified [RCV004337365]	uncertain significance	17	64860790	64860790	Human		name
401871010	CV2756570	single nucleotide variant	NM_001128922.2(LRRC32):c.1691G>A (p.Arg564Gln)	not specified [RCV004345095]	uncertain significance	11	76659902	76659902	Human		name
401883612	CV2758021	single nucleotide variant	NM_001128922.2(LRRC32):c.1958G>A (p.Arg653Gln)	not specified [RCV004339189]	uncertain significance	11	76659635	76659635	Human		name
401866667	CV2758962	single nucleotide variant	NM_199340.5(LRRC37A3):c.3604G>A (p.Glu1202Lys)	not specified [RCV004342277]	likely benign	17	64860542	64860542	Human		name
401857863	CV2766049	single nucleotide variant	NM_199340.5(LRRC37A3):c.3672G>C (p.Glu1224Asp)	not specified [RCV004340508]	uncertain significance	17	64860474	64860474	Human		name
401897776	CV2772902	single nucleotide variant	NM_001321350.2(LRRC37B):c.934C>T (p.Pro312Ser)	not specified [RCV004357675]	uncertain significance	17	32022326	32022326	Human		name
401892147	CV2777273	single nucleotide variant	NM_199340.5(LRRC37A3):c.4636T>C (p.Trp1546Arg)	not specified [RCV004354294]	uncertain significance	17	64859510	64859510	Human		name
401891082	CV2778632	single nucleotide variant	NM_001128922.2(LRRC32):c.1409A>G (p.Glu470Gly)	not specified [RCV004344277]	uncertain significance	11	76660184	76660184	Human		name
401861310	CV2779616	single nucleotide variant	NM_199340.5(LRRC37A3):c.3703C>A (p.Pro1235Thr)	not specified [RCV004351321]	uncertain significance	17	64860443	64860443	Human		name
401885342	CV2783241	single nucleotide variant	NM_199340.5(LRRC37A3):c.3016A>G (p.Lys1006Glu)	not specified [RCV004363859]	likely benign	17	64868499	64868499	Human		name
401876107	CV2789296	single nucleotide variant	NM_001128922.2(LRRC32):c.1498G>A (p.Gly500Ser)	not specified [RCV004365322]	uncertain significance	11	76660095	76660095	Human		name
401882285	CV2793434	single nucleotide variant	NM_199340.5(LRRC37A3):c.3061C>T (p.Pro1021Ser)	not specified [RCV004362525]	uncertain significance	17	64863011	64863011	Human		name
405655534	CV3277268	single nucleotide variant	NM_001128922.2(LRRC32):c.1055G>A (p.Arg352Gln)	not specified [RCV004415421]	uncertain significance	11	76660538	76660538	Human		name
405655542	CV3277271	single nucleotide variant	NM_001128922.2(LRRC32):c.1276G>C (p.Gly426Arg)	not specified [RCV004415424]	uncertain significance	11	76660317	76660317	Human		name
405655545	CV3277272	single nucleotide variant	NM_001128922.2(LRRC32):c.1303G>A (p.Gly435Ser)	not specified [RCV004415425]	likely benign	11	76660290	76660290	Human		name
405655550	CV3277274	single nucleotide variant	NM_001128922.2(LRRC32):c.1591G>T (p.Ala531Ser)	not specified [RCV004415427]	uncertain significance	11	76660002	76660002	Human		name
405655571	CV3277286	single nucleotide variant	NM_001172779.2(LRRC34):c.1270G>A (p.Val424Ile)	not specified [RCV004415439]	uncertain significance	3	169793760	169793760	Human		name
405655714	CV3277347	single nucleotide variant	NM_199340.5(LRRC37A3):c.3032T>C (p.Met1011Thr)	not specified [RCV004415500]	uncertain significance	17	64868483	64868483	Human		name
405655716	CV3277348	single nucleotide variant	NM_199340.5(LRRC37A3):c.3062C>T (p.Pro1021Leu)	not specified [RCV004415501]	uncertain significance	17	64863010	64863010	Human		name
405655717	CV3277349	single nucleotide variant	NM_199340.5(LRRC37A3):c.3100A>G (p.Ser1034Gly)	not specified [RCV004415502]	uncertain significance	17	64862972	64862972	Human		name
405655719	CV3277350	single nucleotide variant	NM_199340.5(LRRC37A3):c.3106G>A (p.Glu1036Lys)	not specified [RCV004415503]	uncertain significance	17	64862966	64862966	Human		name
405655721	CV3277351	single nucleotide variant	NM_199340.5(LRRC37A3):c.3343G>T (p.Asp1115Tyr)	not specified [RCV004415504]	uncertain significance	17	64860803	64860803	Human		name
405655725	CV3277354	single nucleotide variant	NM_199340.5(LRRC37A3):c.3775T>C (p.Ser1259Pro)	not specified [RCV004415507]	uncertain significance	17	64860371	64860371	Human		name
405655727	CV3277355	single nucleotide variant	NM_199340.5(LRRC37A3):c.4118T>G (p.Leu1373Arg)	not specified [RCV004415508]	uncertain significance	17	64860028	64860028	Human		name
405655729	CV3277356	single nucleotide variant	NM_199340.5(LRRC37A3):c.4151A>G (p.Glu1384Gly)	not specified [RCV004415509]	uncertain significance	17	64859995	64859995	Human		name
405655730	CV3277357	single nucleotide variant	NM_199340.5(LRRC37A3):c.4191T>G (p.Phe1397Leu)	not specified [RCV004415510]	uncertain significance	17	64859955	64859955	Human		name
405655732	CV3277358	single nucleotide variant	NM_199340.5(LRRC37A3):c.4259A>G (p.Asn1420Ser)	not specified [RCV004415511]	uncertain significance	17	64859887	64859887	Human		name
405655734	CV3277359	single nucleotide variant	NM_199340.5(LRRC37A3):c.4282G>A (p.Ala1428Thr)	not specified [RCV004415512]	uncertain significance	17	64859864	64859864	Human		name
405655735	CV3277360	single nucleotide variant	NM_199340.5(LRRC37A3):c.4652A>T (p.Tyr1551Phe)	not specified [RCV004415513]	uncertain significance	17	64859494	64859494	Human		name
405655737	CV3277361	single nucleotide variant	NM_199340.5(LRRC37A3):c.4754C>T (p.Ala1585Val)	not specified [RCV004415514]	uncertain significance	17	64858834	64858834	Human		name
405655738	CV3277362	single nucleotide variant	NM_199340.5(LRRC37A3):c.4823G>A (p.Arg1608Gln)	not specified [RCV004415515]	uncertain significance	17	64855876	64855876	Human		name
405655742	CV3277364	single nucleotide variant	NM_001321350.2(LRRC37B):c.827A>G (p.Asn276Ser)	not specified [RCV004415517]	uncertain significance	17	32022219	32022219	Human		name
405655743	CV3277365	single nucleotide variant	NM_001321350.2(LRRC37B):c.881A>G (p.Glu294Gly)	not specified [RCV004415518]	uncertain significance	17	32022273	32022273	Human		name
405655765	CV3277379	single nucleotide variant	NM_001321350.2(LRRC37B):c.404G>A (p.Arg135His)	not specified [RCV004415532]	uncertain significance	17	32021796	32021796	Human		name
405655767	CV3277380	single nucleotide variant	NM_001321350.2(LRRC37B):c.487G>T (p.Ala163Ser)	not specified [RCV004415533]	likely benign	17	32021879	32021879	Human		name
405852916	CV3393344	single nucleotide variant	NM_001128922.2(LRRC32):c.1378G>T (p.Ala460Ser)	not provided [RCV004546074]	likely benign	11	76660215	76660215	Human		name
407500716	CV3456432	single nucleotide variant	NM_001128922.2(LRRC32):c.1943G>C (p.Cys648Ser)	not specified [RCV004644680]	uncertain significance	11	76659650	76659650	Human		name
407500721	CV3456433	single nucleotide variant	NM_001128922.2(LRRC32):c.1165C>T (p.Arg389Trp)	not specified [RCV004644681]	uncertain significance	11	76660428	76660428	Human		name
407500735	CV3456437	single nucleotide variant	NM_001128922.2(LRRC32):c.1501A>G (p.Asn501Asp)	not specified [RCV004644684]	uncertain significance	11	76660092	76660092	Human		name
407500738	CV3456438	single nucleotide variant	NM_001128922.2(LRRC32):c.1384G>A (p.Ala462Thr)	not specified [RCV004644685]	uncertain significance	11	76660209	76660209	Human		name
407468125	CV3456441	single nucleotide variant	NM_001128922.2(LRRC32):c.1748C>T (p.Ala583Val)	not specified [RCV004636162]	uncertain significance	11	76659845	76659845	Human		name
407500754	CV3456443	single nucleotide variant	NM_001128922.2(LRRC32):c.1417C>G (p.Leu473Val)	not specified [RCV004644688]	uncertain significance	11	76660176	76660176	Human		name
407468132	CV3456444	single nucleotide variant	NM_001128922.2(LRRC32):c.1765C>G (p.Arg589Gly)	not specified [RCV004636164]	uncertain significance	11	76659828	76659828	Human		name
407500760	CV3456445	single nucleotide variant	NM_001128922.2(LRRC32):c.1846G>A (p.Glu616Lys)	not specified [RCV004644689]	uncertain significance	11	76659747	76659747	Human		name
407468136	CV3456447	single nucleotide variant	NM_001172779.2(LRRC34):c.1268G>A (p.Arg423His)	not specified [RCV004636165]	likely benign	3	169793762	169793762	Human		name
407485182	CV3456465	single nucleotide variant	NM_001006607.3(LRRC37A2):c.208G>A (p.Glu70Lys)	not specified [RCV004644703]	uncertain significance	17	46512920	46512920	Human		name
407484084	CV3456467	single nucleotide variant	NM_001006607.3(LRRC37A2):c.136C>T (p.Pro46Ser)	not specified [RCV004636171]	uncertain significance	17	46512848	46512848	Human		name
407500787	CV3456469	single nucleotide variant	NM_199340.5(LRRC37A3):c.4654A>T (p.Ile1552Phe)	not specified [RCV004644706]	uncertain significance	17	64859492	64859492	Human		name
407500794	CV3456471	single nucleotide variant	NM_199340.5(LRRC37A3):c.3584C>T (p.Ala1195Val)	not specified [RCV004644708]	uncertain significance	17	64860562	64860562	Human		name
407500809	CV3456475	single nucleotide variant	NM_199340.5(LRRC37A3):c.3071T>A (p.Met1024Lys)	not specified [RCV004644711]	uncertain significance	17	64863001	64863001	Human		name
407468154	CV3456480	single nucleotide variant	NM_199340.5(LRRC37A3):c.3297C>A (p.Asn1099Lys)	not specified [RCV004636173]	uncertain significance	17	64860849	64860849	Human		name
407500852	CV3456486	single nucleotide variant	NM_001321350.2(LRRC37B):c.435G>T (p.Leu145Phe)	not specified [RCV004644721]	uncertain significance	17	32021827	32021827	Human		name
597625975	CV3696793	single nucleotide variant	NM_001128922.2(LRRC32):c.1841G>A (p.Arg614His)	not specified [RCV004938478]	uncertain significance	11	76659752	76659752	Human		name
597625978	CV3696794	single nucleotide variant	NM_001128922.2(LRRC32):c.1288G>A (p.Glu430Lys)	not specified [RCV004938479]	uncertain significance	11	76660305	76660305	Human		name
597626170	CV3696797	single nucleotide variant	NM_001128922.2(LRRC32):c.1955G>A (p.Arg652His)	not specified [RCV004938482]	uncertain significance	11	76659638	76659638	Human		name
597626167	CV3696798	single nucleotide variant	NM_001128922.2(LRRC32):c.1067C>T (p.Ala356Val)	not specified [RCV004938483]	uncertain significance	11	76660526	76660526	Human		name
597626160	CV3696802	single nucleotide variant	NM_001128922.2(LRRC32):c.1700A>T (p.Tyr567Phe)	not specified [RCV004938485]	uncertain significance	11	76659893	76659893	Human		name
597778514	CV3696803	single nucleotide variant	NM_001128922.2(LRRC32):c.1796T>C (p.Ile599Thr)	not specified [RCV004930148]	uncertain significance	11	76659797	76659797	Human		name
597626150	CV3696806	single nucleotide variant	NM_001128922.2(LRRC32):c.1559A>T (p.Asn520Ile)	not specified [RCV004938488]	uncertain significance	11	76660034	76660034	Human		name
597778518	CV3696808	single nucleotide variant	NM_001172779.2(LRRC34):c.1130C>G (p.Thr377Arg)	not specified [RCV004930149]	uncertain significance	3	169795546	169795546	Human		name
597697386	CV3696840	single nucleotide variant	NM_001006607.3(LRRC37A2):c.226A>G (p.Thr76Ala)	not specified [RCV004938513]	uncertain significance	17	46512938	46512938	Human		name
597626096	CV3696847	single nucleotide variant	NM_199340.5(LRRC37A3):c.4877C>T (p.Thr1626Met)	not specified [RCV004938519]	uncertain significance	17	64854627	64854627	Human		name
597625989	CV3696849	single nucleotide variant	NM_199340.5(LRRC37A3):c.3481C>T (p.Arg1161Trp)	not specified [RCV004938521]	uncertain significance	17	64860665	64860665	Human		name
597625994	CV3696852	single nucleotide variant	NM_199340.5(LRRC37A3):c.4877C>G (p.Thr1626Arg)	not specified [RCV004938523]	uncertain significance	17	64854627	64854627	Human		name
597778533	CV3696853	single nucleotide variant	NM_199340.5(LRRC37A3):c.4616T>C (p.Ile1539Thr)	not specified [RCV004930155]	uncertain significance	17	64859530	64859530	Human		name
597626005	CV3696856	single nucleotide variant	NM_199340.5(LRRC37A3):c.4346A>G (p.Asn1449Ser)	not specified [RCV004938526]	uncertain significance	17	64859800	64859800	Human		name
597626008	CV3696857	single nucleotide variant	NM_199340.5(LRRC37A3):c.3265C>T (p.Pro1089Ser)	not specified [RCV004938527]	uncertain significance	17	64860881	64860881	Human		name
597778537	CV3696859	single nucleotide variant	NM_199340.5(LRRC37A3):c.4681G>A (p.Glu1561Lys)	not specified [RCV004930156]	uncertain significance	17	64859465	64859465	Human		name
597626021	CV3696863	single nucleotide variant	NM_199340.5(LRRC37A3):c.4684C>G (p.Gln1562Glu)	not specified [RCV004938531]	uncertain significance	17	64859462	64859462	Human		name
597626028	CV3696866	single nucleotide variant	NM_199340.5(LRRC37A3):c.4561A>G (p.Thr1521Ala)	not specified [RCV004938533]	uncertain significance	17	64859585	64859585	Human		name
597626031	CV3696867	single nucleotide variant	NM_199340.5(LRRC37A3):c.3917G>T (p.Arg1306Leu)	not specified [RCV004938534]	uncertain significance	17	64860229	64860229	Human		name
597626055	CV3696875	single nucleotide variant	NM_001321350.2(LRRC37B):c.796G>A (p.Val266Met)	not specified [RCV004938541]	uncertain significance	17	32022188	32022188	Human		name
597778545	CV3696877	single nucleotide variant	NM_001321350.2(LRRC37B):c.329T>G (p.Leu110Arg)	not specified [RCV004930158]	uncertain significance	17	32021721	32021721	Human		name
597778549	CV3696878	single nucleotide variant	NM_001321350.2(LRRC37B):c.403C>T (p.Arg135Cys)	not specified [RCV004930159]	uncertain significance	17	32021795	32021795	Human		name
597778564	CV3696884	single nucleotide variant	NM_001321350.2(LRRC37B):c.301A>C (p.Thr101Pro)	not specified [RCV004930162]	uncertain significance	17	32021693	32021693	Human		name
598273018	CV3984658	single nucleotide variant	NM_199340.5(LRRC37A3):c.3655A>C (p.Thr1219Pro)	not specified [RCV005350611]	uncertain significance	17	64860491	64860491	Human		name
598250948	CV3984659	single nucleotide variant	NM_199340.5(LRRC37A3):c.3544G>A (p.Val1182Ile)	not specified [RCV005366597]	uncertain significance	17	64860602	64860602	Human		name
598273022	CV3984661	single nucleotide variant	NM_001321350.2(LRRC37B):c.350G>A (p.Arg117His)	not specified [RCV005350612]	likely benign	17	32021742	32021742	Human		name
598250959	CV3984662	single nucleotide variant	NM_001321350.2(LRRC37B):c.466C>T (p.Pro156Ser)	not specified [RCV005366599]	uncertain significance	17	32021858	32021858	Human		name
598250970	CV3984664	single nucleotide variant	NM_001321350.2(LRRC37B):c.664C>A (p.Pro222Thr)	not specified [RCV005366601]	uncertain significance	17	32022056	32022056	Human		name
598250976	CV3984667	single nucleotide variant	NM_001321350.2(LRRC37B):c.478C>T (p.Arg160Trp)	not specified [RCV005366602]	uncertain significance	17	32021870	32021870	Human		name
598231566	CV3984671	single nucleotide variant	NM_001321350.2(LRRC37B):c.740C>G (p.Pro247Arg)	not specified [RCV005362886]	uncertain significance	17	32022132	32022132	Human		name
598250806	CV3988271	single nucleotide variant	NM_001128922.2(LRRC32):c.1592C>T (p.Ala531Val)	not specified [RCV005366574]	uncertain significance	11	76660001	76660001	Human		name
598272889	CV3988272	single nucleotide variant	NM_001128922.2(LRRC32):c.1511T>C (p.Met504Thr)	not specified [RCV005350586]	likely benign	11	76660082	76660082	Human		name
598231523	CV3988273	single nucleotide variant	NM_001128922.2(LRRC32):c.1939G>A (p.Ala647Thr)	not specified [RCV005362879]	likely benign	11	76659654	76659654	Human		name
598231529	CV3988279	single nucleotide variant	NM_001172779.2(LRRC34):c.1060A>G (p.Lys354Glu)	not specified [RCV005362880]	uncertain significance	3	169796218	169796218	Human		name
598272974	CV3988304	single nucleotide variant	NM_001006607.3(LRRC37A2):c.242C>T (p.Pro81Leu)	not specified [RCV005350602]	uncertain significance	17	46512954	46512954	Human		name
598250909	CV3988310	single nucleotide variant	NM_199340.5(LRRC37A3):c.3691G>A (p.Val1231Ile)	not specified [RCV005366591]	uncertain significance	17	64860455	64860455	Human		name
598231549	CV3988312	single nucleotide variant	NM_199340.5(LRRC37A3):c.3985A>C (p.Lys1329Gln)	not specified [RCV005362883]	uncertain significance	17	64860161	64860161	Human		name
598250923	CV3988315	single nucleotide variant	NM_199340.5(LRRC37A3):c.3480C>A (p.Asn1160Lys)	not specified [RCV005366593]	uncertain significance	17	64860666	64860666	Human		name
598250929	CV3988316	single nucleotide variant	NM_199340.5(LRRC37A3):c.4044G>C (p.Lys1348Asn)	not specified [RCV005366594]	uncertain significance	17	64860102	64860102	Human		name
598272988	CV3988317	single nucleotide variant	NM_199340.5(LRRC37A3):c.4084T>G (p.Leu1362Val)	not specified [RCV005350605]	uncertain significance	17	64860062	64860062	Human		name
598272993	CV3988318	single nucleotide variant	NM_199340.5(LRRC37A3):c.3022A>G (p.Ile1008Val)	not specified [RCV005350606]	uncertain significance	17	64868493	64868493	Human		name
598250942	CV3988321	single nucleotide variant	NM_199340.5(LRRC37A3):c.4718T>G (p.Leu1573Arg)	not specified [RCV005366596]	uncertain significance	17	64858870	64858870	Human		name
598273014	CV3988324	single nucleotide variant	NM_199340.5(LRRC37A3):c.3831C>A (p.His1277Gln)	not specified [RCV005350610]	uncertain significance	17	64860315	64860315	Human		name
13832666	CV536136	single nucleotide variant	NM_001128922.2(LRRC32):c.1630C>T (p.Arg544Ter)	Cleft palate, proliferative retinopathy, and developmental delay [RCV001263102]\|Global developmental delay [RCV000735428]	pathogenic\|likely pathogenic	11	76659963	76659963	Human	5	name
15162424	CV704297	single nucleotide variant	NM_199340.5(LRRC37A3):c.4111C>T (p.Pro1371Ser)	not provided [RCV000947851]	benign	17	64860035	64860035	Human		name
15154500	CV715628	single nucleotide variant	NM_199340.5(LRRC37A3):c.3924C>G (p.His1308Gln)	not provided [RCV000968748]	benign	17	64860222	64860222	Human		name
8636295	CV91518	single nucleotide variant	NM_199340.3(LRRC37A3):c.4209G>A (p.Met1403Ile)	Malignant melanoma [RCV000071616]	not provided	17	64859937	64859937	Human		name
155980457	CV2243962	single nucleotide variant	NM_001321350.2(LRRC37B):c.2174G>A (p.Arg725Gln)	not specified [RCV004108460]	uncertain significance	17	32049138	32049138	Human		name
156315590	CV2250792	single nucleotide variant	NM_001321350.2(LRRC37B):c.2124G>C (p.Leu708Phe)	not specified [RCV004129655]	uncertain significance	17	32047888	32047888	Human		name
155925423	CV2258533	single nucleotide variant	NM_001321350.2(LRRC37B):c.1043C>T (p.Thr348Ile)	not specified [RCV004116019]	uncertain significance	17	32022435	32022435	Human		name
155920652	CV2279629	single nucleotide variant	NM_001006607.3(LRRC37A2):c.448C>G (p.Leu150Val)	not specified [RCV004142128]	uncertain significance	17	46513160	46513160	Human		name
156074498	CV2281444	single nucleotide variant	NM_001006607.3(LRRC37A2):c.740C>T (p.Pro247Leu)	not specified [RCV004153772]	uncertain significance	17	46513452	46513452	Human		name
156253373	CV2311452	single nucleotide variant	NM_001321350.2(LRRC37B):c.1081T>G (p.Ser361Ala)	not specified [RCV004168296]	uncertain significance	17	32022473	32022473	Human		name
155911675	CV2313364	single nucleotide variant	NM_001321350.2(LRRC37B):c.2536G>A (p.Val846Met)	not specified [RCV004163690]	uncertain significance	17	32053266	32053266	Human		name
155917882	CV2362442	single nucleotide variant	NM_001006607.3(LRRC37A2):c.599G>A (p.Arg200Gln)	not specified [RCV004213063]	uncertain significance	17	46513311	46513311	Human		name
156087199	CV2366361	single nucleotide variant	NM_001006607.3(LRRC37A2):c.323C>A (p.Pro108Gln)	not specified [RCV004212413]	uncertain significance	17	46513035	46513035	Human		name
156050723	CV2367584	single nucleotide variant	NM_001321350.2(LRRC37B):c.1129A>G (p.Thr377Ala)	not specified [RCV004211512]	uncertain significance	17	32022521	32022521	Human		name
156304965	CV2369291	single nucleotide variant	NM_001321350.2(LRRC37B):c.1759G>A (p.Val587Ile)	not specified [RCV004208204]	uncertain significance	17	32034938	32034938	Human		name
156211889	CV2370404	single nucleotide variant	NM_001321350.2(LRRC37B):c.1942A>C (p.Lys648Gln)	not specified [RCV004213301]	uncertain significance	17	32045764	32045764	Human		name
155993634	CV2377246	single nucleotide variant	NM_001321350.2(LRRC37B):c.1597A>G (p.Ile533Val)	not specified [RCV004232305]	uncertain significance	17	32030675	32030675	Human		name
156147438	CV2377248	single nucleotide variant	NM_001321350.2(LRRC37B):c.2250A>C (p.Glu750Asp)	not specified [RCV004232307]	likely benign	17	32049214	32049214	Human		name
155961379	CV2388025	single nucleotide variant	NM_001321350.2(LRRC37B):c.1498G>A (p.Glu500Lys)	not specified [RCV004241156]	uncertain significance	17	32024775	32024775	Human		name
156202559	CV2392583	single nucleotide variant	NM_001321350.2(LRRC37B):c.2032T>C (p.Phe678Leu)	not specified [RCV004245445]	uncertain significance	17	32047796	32047796	Human		name
155999682	CV2396460	single nucleotide variant	NM_001006607.3(LRRC37A2):c.710C>T (p.Ser237Leu)	not specified [RCV004242170]	likely benign	17	46513422	46513422	Human		name
329382298	CV2424424	single nucleotide variant	NM_001321350.2(LRRC37B):c.1202G>A (p.Arg401Gln)	not specified [RCV004252319]	uncertain significance	17	32022594	32022594	Human		name
329358989	CV2425326	single nucleotide variant	NM_001321350.2(LRRC37B):c.1094C>T (p.Pro365Leu)	not specified [RCV004250991]	uncertain significance	17	32022486	32022486	Human		name
329354765	CV2448977	single nucleotide variant	NM_001321350.2(LRRC37B):c.1100C>T (p.Pro367Leu)	not specified [RCV004264060]	likely benign	17	32022492	32022492	Human		name
329352399	CV2452963	single nucleotide variant	NM_001321350.2(LRRC37B):c.2030C>T (p.Ala677Val)	not specified [RCV004277591]	uncertain significance	17	32047794	32047794	Human		name
329391631	CV2452990	single nucleotide variant	NM_001321350.2(LRRC37B):c.1601G>A (p.Arg534Gln)	not specified [RCV004277614]	likely benign	17	32030679	32030679	Human		name
329388083	CV2468668	single nucleotide variant	NM_001321350.2(LRRC37B):c.2095G>A (p.Ala699Thr)	not specified [RCV004278213]	uncertain significance	17	32047859	32047859	Human		name
401782966	CV2716065	single nucleotide variant	NM_001321350.2(LRRC37B):c.1523A>G (p.Tyr508Cys)	not specified [RCV004323312]	uncertain significance	17	32027786	32027786	Human		name
401856934	CV2755200	single nucleotide variant	NM_001321350.2(LRRC37B):c.1270G>C (p.Glu424Gln)	not specified [RCV004337390]	uncertain significance	17	32022662	32022662	Human		name
401857778	CV2755891	single nucleotide variant	NM_001006607.3(LRRC37A2):c.305C>T (p.Ser102Leu)	not specified [RCV004335984]	likely benign	17	46513017	46513017	Human		name
401865865	CV2775343	single nucleotide variant	NM_001321350.2(LRRC37B):c.1382G>A (p.Arg461His)	not specified [RCV004348751]	likely benign	17	32022774	32022774	Human		name
405655689	CV3277337	single nucleotide variant	NM_001006607.3(LRRC37A2):c.596T>G (p.Leu199Arg)	not specified [RCV004415490]	uncertain significance	17	46513308	46513308	Human		name
405655746	CV3277367	single nucleotide variant	NM_001321350.2(LRRC37B):c.1075G>A (p.Glu359Lys)	not specified [RCV004415520]	uncertain significance	17	32022467	32022467	Human		name
405655753	CV3277371	single nucleotide variant	NM_001321350.2(LRRC37B):c.1541A>G (p.Lys514Arg)	not specified [RCV004415524]	uncertain significance	17	32027804	32027804	Human		name
405655755	CV3277372	single nucleotide variant	NM_001321350.2(LRRC37B):c.1586C>T (p.Ser529Phe)	not specified [RCV004415525]	uncertain significance	17	32030664	32030664	Human		name
405655756	CV3277373	single nucleotide variant	NM_001321350.2(LRRC37B):c.1987A>G (p.Ile663Val)	not specified [RCV004415526]	uncertain significance	17	32045809	32045809	Human		name
407500830	CV3456481	single nucleotide variant	NM_001321350.2(LRRC37B):c.1136T>C (p.Ile379Thr)	not specified [RCV004644716]	likely benign	17	32022528	32022528	Human		name
407500838	CV3456483	single nucleotide variant	NM_001321350.2(LRRC37B):c.1762G>A (p.Glu588Lys)	not specified [RCV004644718]	uncertain significance	17	32034941	32034941	Human		name
407500856	CV3456487	single nucleotide variant	NM_001321350.2(LRRC37B):c.1846A>T (p.Ile616Phe)	not specified [RCV004644722]	uncertain significance	17	32035608	32035608	Human		name
407468157	CV3456489	single nucleotide variant	NM_001321350.2(LRRC37B):c.1387G>C (p.Val463Leu)	not specified [RCV004636174]	uncertain significance	17	32022779	32022779	Human		name
407500862	CV3456490	single nucleotide variant	NM_001321350.2(LRRC37B):c.1393G>A (p.Val465Met)	not specified [RCV004644724]	uncertain significance	17	32022785	32022785	Human		name
597697358	CV3696844	single nucleotide variant	NM_001006607.3(LRRC37A2):c.557G>A (p.Ser186Asn)	not specified [RCV004938516]	uncertain significance	17	46513269	46513269	Human		name
597626041	CV3696870	single nucleotide variant	NM_001321350.2(LRRC37B):c.2426G>C (p.Ser809Thr)	not specified [RCV004938537]	uncertain significance	17	32049390	32049390	Human		name
597626048	CV3696873	single nucleotide variant	NM_001321350.2(LRRC37B):c.2288G>A (p.Arg763Gln)	not specified [RCV004938539]	uncertain significance	17	32049252	32049252	Human		name
597626051	CV3696874	single nucleotide variant	NM_001321350.2(LRRC37B):c.1402C>A (p.Pro468Thr)	not specified [RCV004938540]	uncertain significance	17	32022794	32022794	Human		name
597626057	CV3696876	single nucleotide variant	NM_001321350.2(LRRC37B):c.2479G>A (p.Ala827Thr)	not specified [RCV004938542]	uncertain significance	17	32050051	32050051	Human		name
597778557	CV3696883	single nucleotide variant	NM_001321350.2(LRRC37B):c.1786C>A (p.Pro596Thr)	not specified [RCV004930161]	uncertain significance	17	32034965	32034965	Human		name
598250954	CV3984660	single nucleotide variant	NM_001321350.2(LRRC37B):c.1277C>T (p.Ala426Val)	not specified [RCV005366598]	uncertain significance	17	32022669	32022669	Human		name
598250964	CV3984663	single nucleotide variant	NM_001321350.2(LRRC37B):c.1741C>T (p.Arg581Cys)	not specified [RCV005366600]	uncertain significance	17	32034920	32034920	Human		name
598273026	CV3984665	single nucleotide variant	NM_001321350.2(LRRC37B):c.1879A>G (p.Ile627Val)	not specified [RCV005350613]	uncertain significance	17	32045701	32045701	Human		name
598273030	CV3984669	single nucleotide variant	NM_001321350.2(LRRC37B):c.1922A>G (p.Asn641Ser)	not specified [RCV005350614]	uncertain significance	17	32045744	32045744	Human		name
598273041	CV3984673	single nucleotide variant	NM_001321350.2(LRRC37B):c.1683C>A (p.Ser561Arg)	not specified [RCV005350617]	uncertain significance	17	32031411	32031411	Human		name
598273045	CV3984674	single nucleotide variant	NM_001321350.2(LRRC37B):c.1337A>T (p.Asp446Val)	not specified [RCV005350618]	uncertain significance	17	32022729	32022729	Human		name
598231574	CV3984675	single nucleotide variant	NM_001321350.2(LRRC37B):c.1024A>G (p.Ser342Gly)	not specified [RCV005362887]	uncertain significance	17	32022416	32022416	Human		name
598273049	CV3984676	single nucleotide variant	NM_001321350.2(LRRC37B):c.1954C>G (p.Leu652Val)	not specified [RCV005350619]	uncertain significance	17	32045776	32045776	Human		name
598231578	CV3984678	single nucleotide variant	NM_001321350.2(LRRC37B):c.1723C>T (p.His575Tyr)	not specified [RCV005362888]	uncertain significance	17	32031451	32031451	Human		name
156074481	CV2281443	single nucleotide variant	NM_001006607.3(LRRC37A2):c.1979G>A (p.Arg660Gln)	not specified [RCV004153771]	likely benign	17	46514691	46514691	Human		name
155968630	CV2391480	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2329C>A (p.Pro777Thr)	not specified [RCV004239869]	uncertain significance	17	46515041	46515041	Human		name
156198172	CV2400830	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2466C>G (p.His822Gln)	not specified [RCV004242487]	likely benign	17	46515178	46515178	Human		name
329350464	CV2467087	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2275C>T (p.Pro759Ser)	not specified [RCV004282820]	uncertain significance	17	46514987	46514987	Human		name
401745367	CV2700811	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2676G>C (p.Glu892Asp)	not specified [RCV004307088]	uncertain significance	17	46517428	46517428	Human		name
401745078	CV2710330	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2237C>T (p.Thr746Ile)	not specified [RCV004317504]	uncertain significance	17	46514949	46514949	Human		name
405655632	CV3277316	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2327G>A (p.Arg776His)	not specified [RCV004415469]	likely benign	17	46515039	46515039	Human		name
407485177	CV3456464	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2354G>A (p.Arg785Gln)	not specified [RCV004644702]	uncertain significance	17	46515066	46515066	Human		name
407485195	CV3456468	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2237C>G (p.Thr746Ser)	not specified [RCV004644705]	uncertain significance	17	46514949	46514949	Human		name
597695867	CV3696838	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2197A>G (p.Thr733Ala)	not specified [RCV004930154]	uncertain significance	17	46514909	46514909	Human		name
597697376	CV3696841	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2252T>G (p.Leu751Arg)	not specified [RCV004938514]	uncertain significance	17	46514964	46514964	Human		name
597697367	CV3696843	single nucleotide variant	NM_001006607.3(LRRC37A2):c.2469G>C (p.Lys823Asn)	not specified [RCV004938515]	likely benign	17	46515181	46515181	Human		name
156368342	CV2199824	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3242C>T (p.Thr1081Ile)	not specified [RCV004074022]	uncertain significance	17	46548381	46548381	Human		name
155921604	CV2208514	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3670G>A (p.Glu1224Lys)	not specified [RCV004091045]	uncertain significance	17	46548809	46548809	Human		name
156276667	CV2230572	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3791C>A (p.Ala1264Asp)	not specified [RCV004097539]	uncertain significance	17	46548930	46548930	Human		name
156079016	CV2248420	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3953C>T (p.Thr1318Ile)	not specified [RCV004119560]	uncertain significance	17	46549092	46549092	Human		name
155959690	CV2252555	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3761G>A (p.Gly1254Asp)	not specified [RCV004118444]	uncertain significance	17	46548900	46548900	Human		name
156337721	CV2271169	single nucleotide variant	NM_001006607.3(LRRC37A2):c.5013G>T (p.Lys1671Asn)	not specified [RCV004134533]	uncertain significance	17	46555383	46555383	Human		name
156270119	CV2293466	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3917G>A (p.Arg1306His)	not specified [RCV004152709]	uncertain significance	17	46549056	46549056	Human		name
156008901	CV2294282	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3639G>C (p.Glu1213Asp)	not specified [RCV004151414]	uncertain significance	17	46548778	46548778	Human		name
156348256	CV2312700	single nucleotide variant	NM_001006607.3(LRRC37A2):c.5079G>T (p.Glu1693Asp)	not specified [RCV004169427]	uncertain significance	17	46555555	46555555	Human		name
156190442	CV2339581	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4777A>T (p.Thr1593Ser)	not specified [RCV004194246]	uncertain significance	17	46550487	46550487	Human		name
156192915	CV2344130	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3091T>C (p.Phe1031Leu)	not specified [RCV004195729]	uncertain significance	17	46546292	46546292	Human		name
156212038	CV2366904	single nucleotide variant	NM_001006607.3(LRRC37A2):c.5072C>T (p.Thr1691Met)	not specified [RCV004213317]	uncertain significance	17	46555548	46555548	Human		name
156151394	CV2369158	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3469G>C (p.Val1157Leu)	not specified [RCV004208083]	uncertain significance	17	46548608	46548608	Human		name
156180654	CV2374773	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4269T>G (p.His1423Gln)	not specified [RCV004225377]	uncertain significance	17	46549408	46549408	Human		name
156183090	CV2382199	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3028A>G (p.Met1010Val)	not specified [RCV004228150]	uncertain significance	17	46540856	46540856	Human		name
156133533	CV2382970	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3073G>A (p.Ala1025Thr)	not specified [RCV004217558]	uncertain significance	17	46546274	46546274	Human		name
156142845	CV2383804	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4348G>A (p.Val1450Met)	not specified [RCV004231674]	likely benign	17	46549487	46549487	Human		name
156038629	CV2384189	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4274C>A (p.Ala1425Glu)	not specified [RCV004227585]	uncertain significance	17	46549413	46549413	Human		name
155908391	CV2387307	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3712A>C (p.Thr1238Pro)	not specified [RCV004238395]	uncertain significance	17	46548851	46548851	Human		name
155930126	CV2389312	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3640G>C (p.Val1214Leu)	not specified [RCV004235623]	likely benign	17	46548779	46548779	Human		name
155932147	CV2399964	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3337G>A (p.Glu1113Lys)	not specified [RCV004246894]	uncertain significance	17	46548476	46548476	Human		name
329349461	CV2425070	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3746A>C (p.Lys1249Thr)	not specified [RCV004248966]	uncertain significance	17	46548885	46548885	Human		name
329383141	CV2441910	single nucleotide variant	NM_001006607.3(LRRC37A2):c.5068C>T (p.Pro1690Ser)	not specified [RCV004262091]	uncertain significance	17	46555544	46555544	Human		name
329349989	CV2454758	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4073C>A (p.Ala1358Asp)	not specified [RCV004269989]	uncertain significance	17	46549212	46549212	Human		name
401743747	CV2677697	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3592G>C (p.Glu1198Gln)	not specified [RCV004291780]	uncertain significance	17	46548731	46548731	Human		name
401747713	CV2691332	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4322C>G (p.Thr1441Ser)	not specified [RCV004303084]	uncertain significance	17	46549461	46549461	Human		name
401743089	CV2694052	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4823G>A (p.Arg1608Gln)	not specified [RCV004302489]	uncertain significance	17	46553413	46553413	Human		name
401758378	CV2694073	single nucleotide variant	NM_001006607.3(LRRC37A2):c.5050C>A (p.Pro1684Thr)	not specified [RCV004302508]	uncertain significance	17	46555420	46555420	Human		name
401762313	CV2714096	single nucleotide variant	NM_001006607.3(LRRC37A2):c.5010C>A (p.His1670Gln)	not specified [RCV004317354]	uncertain significance	17	46555380	46555380	Human		name
401748948	CV2716486	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3446A>G (p.Asn1149Ser)	not specified [RCV004325789]	uncertain significance	17	46548585	46548585	Human		name
401749554	CV2723726	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3962T>A (p.Val1321Asp)	not specified [RCV004325891]	uncertain significance	17	46549101	46549101	Human		name
401748612	CV2735377	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3496A>G (p.Arg1166Gly)	not specified [RCV004334031]	uncertain significance	17	46548635	46548635	Human		name
401857396	CV2757960	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3619G>A (p.Gly1207Arg)	not specified [RCV004337092]	likely benign	17	46548758	46548758	Human		name
401857486	CV2779379	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4390C>T (p.Pro1464Ser)	not specified [RCV004351031]	uncertain significance	17	46549529	46549529	Human		name
401858620	CV2780447	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3440C>T (p.Thr1147Ile)	not specified [RCV004358149]	uncertain significance	17	46548579	46548579	Human		name
405655640	CV3277319	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3028A>C (p.Met1010Leu)	not specified [RCV004415472]	uncertain significance	17	46540856	46540856	Human		name
405655643	CV3277320	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3495G>T (p.Lys1165Asn)	not specified [RCV004415473]	likely benign	17	46548634	46548634	Human		name
405655646	CV3277321	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3537C>G (p.Phe1179Leu)	not specified [RCV004415474]	uncertain significance	17	46548676	46548676	Human		name
405655648	CV3277322	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3632C>T (p.Pro1211Leu)	not specified [RCV004415475]	uncertain significance	17	46548771	46548771	Human		name
405655654	CV3277324	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3728C>T (p.Ala1243Val)	not specified [RCV004415477]	uncertain significance	17	46548867	46548867	Human		name
405655657	CV3277325	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3769T>C (p.Ser1257Pro)	not specified [RCV004415478]	uncertain significance	17	46548908	46548908	Human		name
405655660	CV3277326	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3796C>T (p.Pro1266Ser)	not specified [RCV004415479]	uncertain significance	17	46548935	46548935	Human		name
405655665	CV3277328	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3875C>T (p.Thr1292Met)	not specified [RCV004415481]	likely benign	17	46549014	46549014	Human		name
405655668	CV3277329	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3880A>G (p.Thr1294Ala)	not specified [RCV004415482]	likely benign	17	46549019	46549019	Human		name
405655671	CV3277330	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4403C>G (p.Ser1468Cys)	not specified [RCV004415483]	uncertain significance	17	46549542	46549542	Human		name
405655673	CV3277331	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4778C>T (p.Thr1593Met)	not specified [RCV004415484]	likely benign	17	46550488	46550488	Human		name
405655675	CV3277332	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4834C>G (p.Gln1612Glu)	not specified [RCV004415485]	likely benign	17	46553424	46553424	Human		name
405655679	CV3277333	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4966C>T (p.Pro1656Ser)	not specified [RCV004415486]	uncertain significance	17	46555336	46555336	Human		name
405655684	CV3277335	single nucleotide variant	NM_001006607.3(LRRC37A2):c.5053G>C (p.Gly1685Arg)	not specified [RCV004415488]	uncertain significance	17	46555423	46555423	Human		name
407485189	CV3456466	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3912A>T (p.Lys1304Asn)	not specified [RCV004644704]	uncertain significance	17	46549051	46549051	Human		name
597697414	CV3696834	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3692T>C (p.Val1231Ala)	not specified [RCV004938509]	uncertain significance	17	46548831	46548831	Human		name
597697403	CV3696835	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3481C>T (p.Arg1161Trp)	not specified [RCV004938510]	uncertain significance	17	46548620	46548620	Human		name
597695857	CV3696836	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3778A>G (p.Ser1260Gly)	not specified [RCV004930153]	uncertain significance	17	46548917	46548917	Human		name
597697396	CV3696837	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3538A>C (p.Lys1180Gln)	not specified [RCV004938511]	uncertain significance	17	46548677	46548677	Human		name
597626099	CV3696839	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4932T>G (p.Phe1644Leu)	not specified [RCV004938512]	uncertain significance	17	46555302	46555302	Human		name
597697349	CV3696845	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4466A>G (p.Asn1489Ser)	not specified [RCV004938517]	uncertain significance	17	46549605	46549605	Human		name
597697339	CV3696846	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3928A>C (p.Thr1310Pro)	not specified [RCV004938518]	uncertain significance	17	46549067	46549067	Human		name
598272962	CV3988300	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4156A>T (p.Asn1386Tyr)	not specified [RCV005350600]	uncertain significance	17	46549295	46549295	Human		name
598250876	CV3988301	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3948C>A (p.His1316Gln)	not specified [RCV005366586]	uncertain significance	17	46549087	46549087	Human		name
598272967	CV3988302	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3998T>C (p.Leu1333Pro)	not specified [RCV005350601]	uncertain significance	17	46549137	46549137	Human		name
598250882	CV3988303	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4248C>A (p.Asn1416Lys)	not specified [RCV005366587]	uncertain significance	17	46549387	46549387	Human		name
598250887	CV3988306	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4891T>A (p.Cys1631Ser)	not specified [RCV005366588]	uncertain significance	17	46555183	46555183	Human		name
598250894	CV3988307	single nucleotide variant	NM_001006607.3(LRRC37A2):c.4805T>C (p.Ile1602Thr)	not specified [RCV005366589]	uncertain significance	17	46550515	46550515	Human		name
598250901	CV3988308	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3859G>A (p.Ala1287Thr)	not specified [RCV005366590]	uncertain significance	17	46548998	46548998	Human		name
598272979	CV3988309	single nucleotide variant	NM_001006607.3(LRRC37A2):c.3958A>G (p.Lys1320Glu)	not specified [RCV005350603]	uncertain significance	17	46549097	46549097	Human		name

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