fn Variant Search Result - Rat Genome Database

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

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8625902	CV81026	single nucleotide variant	FNIP1:c.2954T>C	Malignant melanoma [RCV000061104]	not provided	5	131670533	131670533	Human		name
150457155	CV1202585	single nucleotide variant	NM_212482.4(FN1):c.*130C>T	not provided [RCV001586238]	likely benign	2	215361425	215361425	Human		name
126920918	CV1041061	single nucleotide variant	NM_212482.4(FN1):c.148+3G>A	not provided [RCV001363166]	uncertain significance	2	215435652	215435652	Human		name
150332933	CV1164185	single nucleotide variant	NM_212482.4(FN1):c.149-3C>T	Glomerulopathy with fibronectin deposits 2 [RCV001702612]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001703008]\|not provided [RCV001692446]\|not specified [RCV001528559]	benign	2	215434827	215434827	Human	2	name
150334953	CV1164186	single nucleotide variant	NM_212482.4(FN1):c.149-4G>T	Glomerulopathy with fibronectin deposits 2 [RCV001703011]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702915]\|not provided [RCV001647364]\|not specified [RCV001529980]	benign	2	215434828	215434828	Human	2	name
151870804	CV1413396	single nucleotide variant	NM_212482.4(FN1):c.685+5G>A	not provided [RCV001998308]	uncertain significance	2	215430710	215430710	Human		name
152159502	CV1522655	single nucleotide variant	NM_212482.4(FN1):c.278-5C>T	not provided [RCV002140673]	likely benign	2	215433466	215433466	Human		name
152124248	CV1563119	single nucleotide variant	NM_212482.4(FN1):c.548-6C>T	not provided [RCV002118237]	likely benign	2	215430858	215430858	Human		name
156359907	CV1910796	single nucleotide variant	NM_212482.4(FN1):c.416-5A>G	not provided [RCV002632603]	likely benign	2	215431969	215431969	Human		name
156016282	CV2120566	single nucleotide variant	NM_212482.4(FN1):c.149-7T>A	not provided [RCV002975920]	likely benign	2	215434831	215434831	Human		name
156205693	CV2401511	single nucleotide variant	NM_212482.4(FN1):c.685+3A>G	Spondylometaphyseal dysplasia - Sutcliffe type [RCV002790041]	likely pathogenic	2	215430712	215430712	Human	1	name
405176758	CV2864506	single nucleotide variant	NM_212482.4(FN1):c.548-9T>G	not provided [RCV003542687]	likely benign	2	215430861	215430861	Human		name
402486438	CV2945161	deletion	NM_212482.4(FN1):c.278-9del	not provided [RCV003660116]	benign	2	215433470	215433470	Human		name
405173730	CV3026937	single nucleotide variant	NM_212482.4(FN1):c.685+1G>A	not provided [RCV003704912]	uncertain significance	2	215430714	215430714	Human		name
597762819	CV3710120	single nucleotide variant	NM_212482.4(FN1):c.416-4A>G	Glomerulopathy with fibronectin deposits 2 [RCV005018576]	uncertain significance	2	215431968	215431968	Human	1	name
597942587	CV3757831	single nucleotide variant	NM_212482.4(FN1):c.547+3G>C	not provided [RCV005077830]	uncertain significance	2	215431830	215431830	Human		name
597942698	CV3757851	single nucleotide variant	NM_212482.4(FN1):c.148+9T>C	not provided [RCV005077850]	likely benign	2	215435646	215435646	Human		name
597894887	CV3773373	single nucleotide variant	NM_212482.4(FN1):c.686-5C>G	not provided [RCV005111280]	likely benign	2	215428343	215428343	Human		name
597931163	CV3789436	single nucleotide variant	NM_212482.4(FN1):c.547+6T>C	not provided [RCV005131717]	uncertain significance	2	215431827	215431827	Human		name
14698131	CV625867	single nucleotide variant	NM_212482.4(FN1):c.685+1G>C	Spondylometaphyseal dysplasia - Sutcliffe type [RCV000790509]	pathogenic	2	215430714	215430714	Human	1	name
126756973	CV1024136	single nucleotide variant	NM_212482.4(FN1):c.2519-5T>A	not provided [RCV001339433]	uncertain significance	2	215407326	215407326	Human		name
126910969	CV1041055	single nucleotide variant	NM_212482.4(FN1):c.2428+2T>C	not provided [RCV001368995]	uncertain significance	2	215408296	215408296	Human		name
127306337	CV1153974	single nucleotide variant	NM_212482.4(FN1):c.5435-7T>C	not provided [RCV001516589]	benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	215379324	215379324	Human		name
127299080	CV1153982	single nucleotide variant	NM_212482.4(FN1):c.1819+7A>T	Glomerulopathy with fibronectin deposits 2 [RCV001702900]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702901]\|not provided [RCV001513543]\|not specified [RCV001529298]	benign	2	215419235	215419235	Human	2	name
127320032	CV1153984	single nucleotide variant	NM_212482.4(FN1):c.547+10T>C	not provided [RCV001522425]	benign\|likely benign	2	215431823	215431823	Human		name
150415733	CV1176094	single nucleotide variant	NM_212482.4(FN1):c.415+90G>T	not provided [RCV001548711]	likely benign	2	215433234	215433234	Human		name
150410664	CV1189803	single nucleotide variant	NM_212482.4(FN1):c.547+19T>C	Glomerulopathy with fibronectin deposits 2 [RCV002495904]\|not provided [RCV001566172]	benign\|likely benign	2	215431814	215431814	Human	1	name
150513798	CV1210693	duplication	NM_212482.4(FN1):c.416-54dup	not provided [RCV001598734]	benign	2	215432007	215432008	Human		name
150448527	CV1214989	single nucleotide variant	NM_212482.4(FN1):c.278-46G>A	not provided [RCV001611578]	benign	2	215433507	215433507	Human		name
150474395	CV1217795	single nucleotide variant	NM_212482.4(FN1):c.149-82G>C	not provided [RCV001615806]	benign	2	215434906	215434906	Human		name
150435471	CV1244419	single nucleotide variant	NM_212482.4(FN1):c.148+89C>T	not provided [RCV001665410]	likely benign	2	215435566	215435566	Human		name
151723015	CV1412409	single nucleotide variant	NM_212482.4(FN1):c.1676-1G>C	not provided [RCV001891368]	uncertain significance	2	215419386	215419386	Human		name
151712524	CV1444696	single nucleotide variant	NM_212482.4(FN1):c.2428+4C>T	not provided [RCV001964576]	uncertain significance	2	215408294	215408294	Human		name
151821245	CV1453556	single nucleotide variant	NM_212482.4(FN1):c.6157+4T>C	Glomerulopathy with fibronectin deposits 2 [RCV002490079]\|not provided [RCV001879234]	likely benign\|uncertain significance	2	215375210	215375210	Human	1	name
151760857	CV1459549	single nucleotide variant	NM_212482.4(FN1):c.4343-9G>T	not provided [RCV002044260]	uncertain significance	2	215386967	215386967	Human		name
151724801	CV1496687	single nucleotide variant	NM_212482.4(FN1):c.5164+3A>G	Glomerulopathy with fibronectin deposits 2 [RCV002484445]\|not provided [RCV001910198]	uncertain significance	2	215382209	215382209	Human	1	name
151731391	CV1512136	single nucleotide variant	NM_212482.4(FN1):c.2122+4T>C	Glomerulopathy with fibronectin deposits 2 [RCV005017087]\|not provided [RCV002021332]	uncertain significance	2	215409930	215409930	Human	1	name
152127180	CV1530241	single nucleotide variant	NM_212482.4(FN1):c.416-17C>T	Glomerulopathy with fibronectin deposits 2 [RCV002505875]\|not provided [RCV002198834]	benign\|likely benign	2	215431981	215431981	Human	1	name
152033263	CV1542644	single nucleotide variant	NM_212482.4(FN1):c.416-16G>A	not provided [RCV002106534]	likely benign	2	215431980	215431980	Human		name
152153089	CV1545256	single nucleotide variant	NM_212482.4(FN1):c.148+16G>A	Glomerulopathy with fibronectin deposits 2 [RCV002508089]\|not provided [RCV002139819]	benign\|likely benign	2	215435639	215435639	Human	1	name
152169828	CV1546606	single nucleotide variant	NM_212482.4(FN1):c.1676-9G>A	Glomerulopathy with fibronectin deposits 2 [RCV002508095]\|not provided [RCV002142916]	benign\|likely benign	2	215419394	215419394	Human	1	name
152120046	CV1547323	single nucleotide variant	NM_212482.4(FN1):c.3605-4C>G	not provided [RCV002081428]	likely benign	2	215394723	215394723	Human		name
152171509	CV1552775	single nucleotide variant	NM_212482.4(FN1):c.1037-8G>A	not provided [RCV002143470]	likely benign	2	215424333	215424333	Human		name
152031526	CV1561236	single nucleotide variant	NM_212482.4(FN1):c.278-18C>T	Glomerulopathy with fibronectin deposits 2 [RCV002500148]\|not provided [RCV002106178]	likely benign	2	215433479	215433479	Human	1	name
152070030	CV1579663	single nucleotide variant	NM_212482.4(FN1):c.278-14C>G	not provided [RCV002074977]	likely benign	2	215433475	215433475	Human		name
152125152	CV1580650	single nucleotide variant	NM_212482.4(FN1):c.7251+7C>G	not provided [RCV002082109]	likely benign	2	215364872	215364872	Human		name
152043005	CV1621787	single nucleotide variant	NM_212482.4(FN1):c.5977+7A>G	Glomerulopathy with fibronectin deposits 2 [RCV002486886]\|not provided [RCV002107994]	likely benign	2	215375622	215375622	Human	1	name
152140453	CV1625139	single nucleotide variant	NM_212482.4(FN1):c.548-10T>C	Glomerulopathy with fibronectin deposits 2 [RCV002507925]\|not provided [RCV002219300]	likely benign	2	215430862	215430862	Human	1	name
152166955	CV1632775	single nucleotide variant	NM_212482.4(FN1):c.277+17C>T	not provided [RCV002182044]	likely benign	2	215434679	215434679	Human		name
152074614	CV1638253	single nucleotide variant	NM_212482.4(FN1):c.3518-4A>G	not provided [RCV002192246]	likely benign	2	215397227	215397227	Human		name
152159857	CV1642261	single nucleotide variant	NM_212482.4(FN1):c.6158-7C>T	Glomerulopathy with fibronectin deposits 2 [RCV002499956]\|not provided [RCV002103590]	likely benign	2	215373418	215373418	Human	1	name
152039868	CV1644019	single nucleotide variant	NM_212482.4(FN1):c.2714-7C>T	not provided [RCV002125928]	likely benign	2	215406517	215406517	Human		name
152083621	CV1647912	single nucleotide variant	NM_212482.4(FN1):c.5051-9C>A	Glomerulopathy with fibronectin deposits 2 [RCV002498102]\|not provided [RCV002076698]	likely benign	2	215382334	215382334	Human	1	name
152048613	CV1655999	single nucleotide variant	NM_212482.4(FN1):c.844+14C>T	not provided [RCV002207229]	likely benign	2	215428166	215428166	Human		name
152110021	CV1665230	single nucleotide variant	NM_212482.4(FN1):c.844+13A>G	not provided [RCV002080118]	likely benign	2	215428167	215428167	Human		name
153349846	CV1693177	single nucleotide variant	NM_212482.4(FN1):c.7251+5G>T	not provided [RCV002276277]	uncertain significance	2	215364874	215364874	Human		name
155266201	CV1698843	single nucleotide variant	NM_212482.4(FN1):c.7144+1G>A	Glomerulopathy with fibronectin deposits 2 [RCV002281673]	likely pathogenic	2	215365504	215365504	Human	1	name
156340746	CV1898763	single nucleotide variant	NM_212482.4(FN1):c.5164+4C>T	Glomerulopathy with fibronectin deposits 2 [RCV005021552]\|not provided [RCV003090346]	uncertain significance	2	215382208	215382208	Human	1	name
156379489	CV1903372	duplication	NM_212482.4(FN1):c.4613-5dup	not provided [RCV003093160]	benign	2	215384980	215384981	Human		name
156215704	CV1910583	single nucleotide variant	NM_212482.4(FN1):c.4070-8G>A	not provided [RCV002596253]	likely benign	2	215391822	215391822	Human		name
156408077	CV1911452	single nucleotide variant	NM_212482.4(FN1):c.6248-7C>T	not provided [RCV002607110]	likely benign	2	215372382	215372382	Human		name
156186222	CV1919206	duplication	NM_212482.4(FN1):c.3349-6dup	not provided [RCV002595225]	likely benign	2	215397853	215397854	Human		name
156202294	CV1952540	single nucleotide variant	NM_212482.4(FN1):c.1036+5G>A	not provided [RCV002574822]	uncertain significance	2	215425089	215425089	Human		name
156234213	CV1952704	single nucleotide variant	NM_212482.4(FN1):c.148+16G>C	not provided [RCV002575990]	likely benign	2	215435639	215435639	Human		name
156167682	CV1959976	single nucleotide variant	NM_212482.4(FN1):c.1675+9C>A	not provided [RCV002573718]	likely benign	2	215420664	215420664	Human		name
156407109	CV1963907	single nucleotide variant	NM_212482.4(FN1):c.3604+9G>C	not provided [RCV002586124]	likely benign	2	215397128	215397128	Human		name
156117431	CV1972893	duplication	NM_212482.4(FN1):c.7019-5dup	not provided [RCV002593001]	likely benign	2	215365634	215365635	Human		name
156235665	CV1976851	single nucleotide variant	NM_212482.4(FN1):c.3349-1G>T	not provided [RCV002596969]	uncertain significance	2	215397849	215397849	Human		name
156084745	CV1987541	single nucleotide variant	NM_212482.4(FN1):c.6854-4A>G	not provided [RCV002621659]	likely benign	2	215368031	215368031	Human		name
156223786	CV2005865	single nucleotide variant	NM_212482.4(FN1):c.7019-4A>G	not provided [RCV002667325]	likely benign	2	215365634	215365634	Human		name
156123909	CV2021099	single nucleotide variant	NM_212482.4(FN1):c.685+17T>A	not provided [RCV002740305]	likely benign	2	215430698	215430698	Human		name
156254532	CV2041204	single nucleotide variant	NM_212482.4(FN1):c.3348+8G>A	not provided [RCV002806122]	likely benign	2	215399249	215399249	Human		name
155902018	CV2043652	single nucleotide variant	NM_212482.4(FN1):c.4729+9G>A	not provided [RCV002771034]	likely benign	2	215384851	215384851	Human		name
156085337	CV2095069	single nucleotide variant	NM_212482.4(FN1):c.5164+9C>T	not provided [RCV002912843]	likely benign	2	215382203	215382203	Human		name
156222651	CV2115204	single nucleotide variant	NM_212482.4(FN1):c.4070-9C>T	not provided [RCV002932518]	likely benign	2	215391823	215391823	Human		name
156016317	CV2120568	single nucleotide variant	NM_212482.4(FN1):c.149-10T>A	not provided [RCV002975922]	likely benign	2	215434834	215434834	Human		name
156279037	CV2137443	single nucleotide variant	NM_212482.4(FN1):c.6158-8C>A	not provided [RCV003009532]	likely benign	2	215373419	215373419	Human		name
156094188	CV2139414	single nucleotide variant	NM_212482.4(FN1):c.2428+6T>C	not provided [RCV002979727]	uncertain significance	2	215408292	215408292	Human		name
156293990	CV2152839	single nucleotide variant	NM_212482.4(FN1):c.1037-8G>C	not provided [RCV003010084]	likely benign	2	215424333	215424333	Human		name
156070547	CV2172592	single nucleotide variant	NM_212482.4(FN1):c.547+12T>G	not provided [RCV003053704]	likely benign	2	215431821	215431821	Human		name
156030438	CV2182074	single nucleotide variant	NM_212482.4(FN1):c.3254-4A>T	not provided [RCV003036161]	uncertain significance	2	215399355	215399355	Human		name
401908696	CV2801402	single nucleotide variant	NM_212482.4(FN1):c.3517+1G>A	FN1-related disorder [RCV003397644]\|Glomerulopathy with fibronectin deposits 2 [RCV005021942]	uncertain significance	2	215397679	215397679	Human	2	name , alternate_id
405176245	CV2864689	single nucleotide variant	NM_212482.4(FN1):c.4342+2T>C	Glomerulopathy with fibronectin deposits 2 [RCV005022007]\|not provided [RCV003542784]	uncertain significance	2	215388210	215388210	Human	1	name
405095393	CV2874892	single nucleotide variant	NM_212482.4(FN1):c.5888-5C>G	not provided [RCV003550221]	likely benign	2	215375723	215375723	Human		name
405198308	CV2880214	single nucleotide variant	NM_212482.4(FN1):c.4069+3G>A	not provided [RCV003551015]	uncertain significance	2	215392928	215392928	Human		name
405238009	CV2881369	single nucleotide variant	NM_212482.4(FN1):c.416-19T>A	not provided [RCV003556784]	likely benign	2	215431983	215431983	Human		name
405186017	CV2921372	single nucleotide variant	NM_212482.4(FN1):c.7362+4A>C	not provided [RCV003564461]	uncertain significance	2	215361965	215361965	Human		name
402486721	CV2945200	single nucleotide variant	NM_212482.4(FN1):c.7362+8C>G	not provided [RCV003660144]	likely benign	2	215361961	215361961	Human		name
405083763	CV2946407	duplication	NM_212482.4(FN1):c.7362+2dup	not provided [RCV003664806]	uncertain significance	2	215361966	215361967	Human		name
405246407	CV2965777	single nucleotide variant	NM_212482.4(FN1):c.2429-5C>T	not provided [RCV003685392]	likely benign	2	215408202	215408202	Human		name
405246411	CV2965778	single nucleotide variant	NM_212482.4(FN1):c.2429-9C>T	not provided [RCV003685393]	likely benign	2	215408206	215408206	Human		name
405147579	CV3024047	single nucleotide variant	NM_212482.4(FN1):c.5978-5T>G	not provided [RCV003702994]	uncertain significance	2	215375398	215375398	Human		name
405144826	CV3052239	single nucleotide variant	NM_212482.4(FN1):c.7019-7C>T	not provided [RCV003725960]	likely benign	2	215365637	215365637	Human		name
405189204	CV3121378	single nucleotide variant	NM_212482.4(FN1):c.1217-8C>A	Glomerulopathy with fibronectin deposits 2 [RCV005014999]\|not provided [RCV003820834]	likely benign\|uncertain significance	2	215423534	215423534	Human	1	name
405027500	CV3129763	single nucleotide variant	NM_212482.4(FN1):c.5435-6C>T	not provided [RCV003830361]	likely benign	2	215379323	215379323	Human		name
405096004	CV3134967	single nucleotide variant	NM_212482.4(FN1):c.1393+7T>A	not provided [RCV003835119]	likely benign	2	215423343	215423343	Human		name
405083513	CV3137432	single nucleotide variant	NM_212482.4(FN1):c.5051-1G>A	not provided [RCV003834141]	uncertain significance	2	215382326	215382326	Human		name
405043412	CV3141292	single nucleotide variant	NM_212482.4(FN1):c.6714+9T>C	not provided [RCV003831585]	likely benign	2	215371900	215371900	Human		name
405149146	CV3152429	single nucleotide variant	NM_212482.4(FN1):c.3254-7C>T	not provided [RCV003856208]	likely benign	2	215399358	215399358	Human		name
405135528	CV3164014	single nucleotide variant	NM_212482.4(FN1):c.844+15G>A	not provided [RCV003855002]	likely benign	2	215428165	215428165	Human		name
402500289	CV3170503	single nucleotide variant	NM_212482.4(FN1):c.547+18C>G	not provided [RCV003877876]	uncertain significance	2	215431815	215431815	Human		name
402484338	CV3171251	single nucleotide variant	NM_212482.4(FN1):c.4613-4C>T	not provided [RCV003876278]	likely benign	2	215384980	215384980	Human		name
404993536	CV3176461	single nucleotide variant	NM_212482.4(FN1):c.6158-9T>C	not provided [RCV003881893]	likely benign	2	215373420	215373420	Human		name
405270180	CV3187638	single nucleotide variant	NM_212482.4(FN1):c.3253+4A>C	not provided [RCV003887722]	uncertain significance	2	215404385	215404385	Human		name
408373876	CV3513024	single nucleotide variant	NM_212482.4(FN1):c.6248-9C>A	FN1-related disorder [RCV004745772]	likely benign	2	215372384	215372384	Human		name , trait , alternate_id
597634775	CV3709989	single nucleotide variant	NM_212482.4(FN1):c.6158-6C>G	Glomerulopathy with fibronectin deposits 2 [RCV005024005]	uncertain significance	2	215373417	215373417	Human	1	name
597634813	CV3710014	single nucleotide variant	NM_212482.4(FN1):c.5165-9G>T	Glomerulopathy with fibronectin deposits 2 [RCV005024011]	uncertain significance	2	215381089	215381089	Human	1	name
597634832	CV3710026	single nucleotide variant	NM_212482.4(FN1):c.4730-6A>T	Glomerulopathy with fibronectin deposits 2 [RCV005024014]	uncertain significance	2	215384190	215384190	Human	1	name
597762585	CV3710050	single nucleotide variant	NM_212482.4(FN1):c.3797-1G>A	Glomerulopathy with fibronectin deposits 2 [RCV005018530]	uncertain significance	2	215393204	215393204	Human	1	name
597762649	CV3710067	single nucleotide variant	NM_212482.4(FN1):c.3254-1G>C	Glomerulopathy with fibronectin deposits 2 [RCV005018542]	uncertain significance	2	215399352	215399352	Human	1	name
597762678	CV3710082	single nucleotide variant	NM_212482.4(FN1):c.2428+9G>A	Glomerulopathy with fibronectin deposits 2 [RCV005018548]	uncertain significance	2	215408289	215408289	Human	1	name
597762768	CV3710108	single nucleotide variant	NM_212482.4(FN1):c.1036+3A>G	Glomerulopathy with fibronectin deposits 2 [RCV005018566]	uncertain significance	2	215425091	215425091	Human	1	name
597839595	CV3737045	deletion	NM_212482.4(FN1):c.5623-7del	not provided [RCV005064525]	likely benign	2	215378269	215378269	Human		name
597836058	CV3739771	single nucleotide variant	NM_212482.4(FN1):c.7144+4T>C	not provided [RCV005063991]	uncertain significance	2	215365501	215365501	Human		name
597838111	CV3740281	single nucleotide variant	NM_212482.4(FN1):c.7362+9A>G	not provided [RCV005064309]	likely benign	2	215361960	215361960	Human		name
597850762	CV3746940	single nucleotide variant	NM_212482.4(FN1):c.6248-7C>G	not provided [RCV005060568]	likely benign	2	215372382	215372382	Human		name
597836735	CV3757736	single nucleotide variant	NM_212482.4(FN1):c.415+18T>C	not provided [RCV005085750]	likely benign	2	215433306	215433306	Human		name
597896824	CV3806730	single nucleotide variant	NM_212482.4(FN1):c.416-13G>C	not provided [RCV005152117]	likely benign	2	215431977	215431977	Human		name
597839234	CV3824917	single nucleotide variant	NM_212482.4(FN1):c.3349-7C>T	not provided [RCV005171781]	likely benign	2	215397855	215397855	Human		name
597841846	CV3825598	single nucleotide variant	NM_212482.4(FN1):c.4342+9T>C	not provided [RCV005172281]	likely benign	2	215388203	215388203	Human		name
597945026	CV3844145	single nucleotide variant	NM_212482.4(FN1):c.4252+9T>C	not provided [RCV005188754]	likely benign	2	215391623	215391623	Human		name
597954085	CV3844338	single nucleotide variant	NM_212482.4(FN1):c.1216+3G>A	not provided [RCV005191011]	uncertain significance	2	215424143	215424143	Human		name
597874798	CV3859672	single nucleotide variant	NM_212482.4(FN1):c.6714+1G>A	not provided [RCV005198076]	uncertain significance	2	215371908	215371908	Human		name
597921407	CV3861758	single nucleotide variant	NM_212482.4(FN1):c.277+10A>C	not provided [RCV005205134]	likely benign	2	215434686	215434686	Human		name
15152457	CV730105	single nucleotide variant	NM_212482.4(FN1):c.3604+9G>A	not provided [RCV000879811]	benign	2	215397128	215397128	Human		name
15198854	CV730106	single nucleotide variant	NM_212482.4(FN1):c.3517+3A>G	not provided [RCV000890474]	benign\|likely benign	2	215397677	215397677	Human		name
15199896	CV730107	single nucleotide variant	NM_212482.4(FN1):c.1547-6A>G	Glomerulopathy with fibronectin deposits 2 [RCV002501462]\|not provided [RCV000890761]	benign\|likely benign	2	215420807	215420807	Human	1	name
15175939	CV743862	single nucleotide variant	NM_212482.4(FN1):c.3254-5C>T	not provided [RCV000906325]	likely benign	2	215399356	215399356	Human		name
15193193	CV777185	single nucleotide variant	NM_212482.4(FN1):c.7018+7A>G	not provided [RCV000955300]	benign	2	215367856	215367856	Human		name
126756624	CV988357	single nucleotide variant	NM_212482.4(FN1):c.2299+3A>T	Glomerulopathy with fibronectin deposits 2 [RCV002486205]\|not provided [RCV001308167]	uncertain significance	2	215409560	215409560	Human	1	name
126909781	CV1037141	single nucleotide variant	NM_212482.4(FN1):c.6853+12C>G	not provided [RCV001354069]	benign\|uncertain significance	2	215370282	215370282	Human		name
150339785	CV1164184	single nucleotide variant	NM_212482.4(FN1):c.2518+12G>C	Glomerulopathy with fibronectin deposits 2 [RCV001703009]\|Glomerulopathy with fibronectin deposits 2 [RCV002501862]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001703010]\|not provided [RCV001535099]\|not specified [RCV001529205]	benign\|likely benign	2	215408096	215408096	Human	2	name
150331489	CV1170891	single nucleotide variant	NM_212482.4(FN1):c.845-194A>G	not provided [RCV001538653]	likely benign	2	215425479	215425479	Human		name
150412995	CV1176092	single nucleotide variant	NM_212482.4(FN1):c.1675+35A>G	not provided [RCV001547666]	likely benign	2	215420638	215420638	Human		name
150422683	CV1179438	single nucleotide variant	NM_212482.4(FN1):c.7363-44C>T	not provided [RCV001552968]	likely benign	2	215361670	215361670	Human		name
150427479	CV1186378	single nucleotide variant	NM_212482.4(FN1):c.1394-55A>G	not provided [RCV001560980]	likely benign	2	215422298	215422298	Human		name
150418336	CV1193060	single nucleotide variant	NM_212482.4(FN1):c.7363-30A>G	not provided [RCV001569171]	likely benign	2	215361656	215361656	Human		name
150420276	CV1193062	single nucleotide variant	NM_212482.4(FN1):c.3797-44A>G	not provided [RCV001570047]	likely benign	2	215393247	215393247	Human		name
150418194	CV1193065	single nucleotide variant	NM_212482.4(FN1):c.1037-21C>G	not provided [RCV001569105]	likely benign	2	215424346	215424346	Human		name
150420052	CV1193066	single nucleotide variant	NM_212482.4(FN1):c.845-250A>G	not provided [RCV001569948]	likely benign	2	215425535	215425535	Human		name
150421669	CV1196815	duplication	NM_212482.4(FN1):c.7363-72dup	not provided [RCV001578135]	likely benign	2	215361694	215361695	Human		name
150415108	CV1196817	deletion	NM_212482.4(FN1):c.4343-29del	not provided [RCV001575251]	likely benign	2	215386987	215386987	Human		name
150418198	CV1196818	single nucleotide variant	NM_212482.4(FN1):c.4069+21C>T	not provided [RCV001576639]	likely benign	2	215392910	215392910	Human		name
150432301	CV1200600	single nucleotide variant	NM_212482.4(FN1):c.5165-88T>A	not provided [RCV001581323]	likely benign	2	215381168	215381168	Human		name
150437923	CV1201332	single nucleotide variant	NM_212482.4(FN1):c.7362+62C>G	not provided [RCV001583144]	benign\|likely benign	2	215361907	215361907	Human		name
150447816	CV1201941	single nucleotide variant	NM_212482.4(FN1):c.2300-53C>T	not provided [RCV001584810]	likely benign	2	215408479	215408479	Human		name
150474414	CV1202096	deletion	NM_212482.4(FN1):c.7251+78del	not provided [RCV001589339]	likely benign	2	215364801	215364801	Human		name
150430966	CV1204066	single nucleotide variant	NM_212482.4(FN1):c.6853+36C>G	not provided [RCV001580841]	likely benign	2	215370258	215370258	Human		name
150495869	CV1205924	single nucleotide variant	NM_212482.4(FN1):c.3797-24T>C	not provided [RCV001593606]	likely benign	2	215393227	215393227	Human		name
150463749	CV1206776	single nucleotide variant	NM_212482.4(FN1):c.6853+29G>A	not provided [RCV001587177]	likely benign	2	215370265	215370265	Human		name
150499371	CV1209071	single nucleotide variant	NM_212482.4(FN1):c.2300-63G>T	not provided [RCV001594289]	likely benign	2	215408489	215408489	Human		name
150514105	CV1210861	single nucleotide variant	NM_212482.4(FN1):c.3253+81C>A	not provided [RCV001598903]	benign	2	215404308	215404308	Human		name
150503227	CV1212433	single nucleotide variant	NM_212482.4(FN1):c.2518+62C>T	not provided [RCV001595308]	benign	2	215408046	215408046	Human		name
150511622	CV1212793	single nucleotide variant	NM_212482.4(FN1):c.7362+50T>G	not provided [RCV001598025]	benign	2	215361919	215361919	Human		name
150511633	CV1212796	single nucleotide variant	NM_212482.4(FN1):c.845-139A>T	not provided [RCV001598028]	benign	2	215425424	215425424	Human		name
150448590	CV1214998	single nucleotide variant	NM_212482.4(FN1):c.3349-50T>G	not provided [RCV001611587]	benign	2	215397898	215397898	Human		name
150450691	CV1215273	single nucleotide variant	NM_212482.4(FN1):c.3348+54G>T	not provided [RCV001611863]	benign	2	215399203	215399203	Human		name
150433708	CV1216993	single nucleotide variant	NM_212482.4(FN1):c.4613-51T>C	not provided [RCV001608895]	benign	2	215385027	215385027	Human		name
150433827	CV1217022	single nucleotide variant	NM_153756.3(FNDC5):c.*1730C>T	not provided [RCV001608924]	benign	1	32862564	32862564	Human		name
150466597	CV1218216	single nucleotide variant	NM_212482.4(FN1):c.7018+30G>T	not provided [RCV001614342]	benign	2	215367833	215367833	Human		name
150469254	CV1219043	single nucleotide variant	NM_212482.4(FN1):c.844+126T>C	not provided [RCV001614795]	benign	2	215428054	215428054	Human		name
150469844	CV1219141	single nucleotide variant	NM_212482.4(FN1):c.4252+11G>C	not provided [RCV001614893]	benign	2	215391621	215391621	Human		name
150514060	CV1228035	single nucleotide variant	NM_212482.4(FN1):c.5711-45G>A	not provided [RCV001638313]	benign	2	215376719	215376719	Human		name
150430735	CV1231027	single nucleotide variant	NM_212482.4(FN1):c.3605-37C>T	not provided [RCV001641576]	benign	2	215394756	215394756	Human		name
150444690	CV1233053	single nucleotide variant	NM_212482.4(FN1):c.277+138T>G	not provided [RCV001645726]	benign	2	215434558	215434558	Human		name
150500517	CV1234655	single nucleotide variant	NM_212482.4(FN1):c.148+193G>A	not provided [RCV001656622]	benign	2	215435462	215435462	Human	4	name
150461641	CV1234805	deletion	NM_212482.4(FN1):c.3797-24del	not provided [RCV001649387]	benign	2	215393227	215393227	Human		name
150457987	CV1237152	single nucleotide variant	NM_212482.4(FN1):c.6715-87A>C	not provided [RCV001648831]	benign	2	215370519	215370519	Human		name
150435981	CV1238133	single nucleotide variant	NM_212482.4(FN1):c.3253+17G>A	Glomerulopathy with fibronectin deposits 2 [RCV001703034]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702220]\|not provided [RCV001654979]	benign	2	215404372	215404372	Human	2	name
150500664	CV1238223	single nucleotide variant	NM_212482.4(FN1):c.1216+30T>G	not provided [RCV001656653]	benign	2	215424116	215424116	Human		name
150493340	CV1238651	single nucleotide variant	NM_212482.4(FN1):c.6158-34T>C	not provided [RCV001655195]	benign	2	215373445	215373445	Human		name
150438399	CV1239750	single nucleotide variant	NM_212482.4(FN1):c.5622+21A>G	Glomerulopathy with fibronectin deposits 2 [RCV001703150]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001703037]\|not provided [RCV001652913]	benign	2	215379109	215379109	Human	2	name
150478254	CV1240162	single nucleotide variant	NM_212482.4(FN1):c.1036+34G>T	not provided [RCV001652340]	benign	2	215425060	215425060	Human		name
150503404	CV1241799	single nucleotide variant	NM_212482.4(FN1):c.685+246C>A	not provided [RCV001657390]	benign	2	215430469	215430469	Human		name
150470870	CV1248094	single nucleotide variant	NM_212482.4(FN1):c.3517+56A>G	not provided [RCV001671130]	benign	2	215397624	215397624	Human		name
150445327	CV1248286	single nucleotide variant	NM_212482.4(FN1):c.2986+27C>T	not provided [RCV001666992]	benign	2	215406211	215406211	Human		name
150443682	CV1249313	single nucleotide variant	NM_212482.4(FN1):c.547+299C>G	not provided [RCV001666745]	benign	2	215431534	215431534	Human		name
150437150	CV1249822	single nucleotide variant	NM_212482.4(FN1):c.1216+92C>T	not provided [RCV001665736]	benign	2	215424054	215424054	Human		name
150474393	CV1251272	single nucleotide variant	NM_212482.4(FN1):c.3349-20C>G	not provided [RCV001671766]	benign	2	215397868	215397868	Human		name
150487912	CV1251593	single nucleotide variant	NM_212482.4(FN1):c.4070-78A>G	not provided [RCV001674264]	benign	2	215391892	215391892	Human		name
150464292	CV1252653	single nucleotide variant	NM_212482.4(FN1):c.2713+87T>A	not provided [RCV001669977]	benign	2	215407040	215407040	Human		name
150451424	CV1260257	single nucleotide variant	NM_212482.4(FN1):c.685+126A>T	not provided [RCV001680747]	benign	2	215430589	215430589	Human		name
150453329	CV1260501	single nucleotide variant	NM_212482.4(FN1):c.1216+28A>G	not provided [RCV001680992]	benign	2	215424118	215424118	Human		name
150450234	CV1260932	duplication	NM_212482.4(FN1):c.3348+41dup	not provided [RCV001680601]	benign	2	215399215	215399216	Human		name
150445947	CV1261285	single nucleotide variant	NM_212482.4(FN1):c.416-173C>T	not provided [RCV001679959]	benign	2	215432137	215432137	Human		name
150446328	CV1261348	single nucleotide variant	NM_212482.4(FN1):c.3253+79A>C	not provided [RCV001680022]	benign	2	215404310	215404310	Human		name
150483153	CV1261737	single nucleotide variant	NM_212482.4(FN1):c.3253+66C>A	not provided [RCV001686341]	benign	2	215404323	215404323	Human		name
150473287	CV1262877	single nucleotide variant	NM_212482.4(FN1):c.278-229T>G	not provided [RCV001684693]	benign	2	215433690	215433690	Human		name
150438718	CV1264865	single nucleotide variant	NM_212482.4(FN1):c.7018+30G>A	not provided [RCV001678858]	benign	2	215367833	215367833	Human		name
150439164	CV1264932	single nucleotide variant	NM_212482.4(FN1):c.5435-35A>G	not provided [RCV001678925]	benign	2	215379352	215379352	Human		name
150493403	CV1267139	single nucleotide variant	NM_212482.4(FN1):c.415+172C>T	not provided [RCV001688166]	benign	2	215433152	215433152	Human		name
150459454	CV1268345	single nucleotide variant	NM_212482.4(FN1):c.3348+23C>G	not provided [RCV001693342]	benign	2	215399234	215399234	Human		name
150460579	CV1269822	single nucleotide variant	NM_212482.4(FN1):c.415+251C>G	not provided [RCV001693525]	benign	2	215433073	215433073	Human		name
150499614	CV1270853	single nucleotide variant	NM_212482.4(FN1):c.685+157C>T	not provided [RCV001689403]	benign	2	215430558	215430558	Human		name
150473695	CV1272213	single nucleotide variant	NM_212482.4(FN1):c.1217-36A>T	not provided [RCV001695751]	benign	2	215423562	215423562	Human		name
150473704	CV1272214	single nucleotide variant	NM_212482.4(FN1):c.1216+74C>T	not provided [RCV001695752]	benign	2	215424072	215424072	Human		name
150449517	CV1273644	single nucleotide variant	NM_212482.4(FN1):c.277+298A>G	not provided [RCV001691744]	benign	2	215434398	215434398	Human		name
150436107	CV1273902	single nucleotide variant	NM_212482.4(FN1):c.4253-15C>G	Glomerulopathy with fibronectin deposits 2 [RCV001702246]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001703164]\|not provided [RCV001698624]	benign	2	215388316	215388316	Human	2	name
150450385	CV1275121	single nucleotide variant	NM_212482.4(FN1):c.4343-16C>T	Glomerulopathy with fibronectin deposits 2 [RCV001702194]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702034]\|not provided [RCV001713690]	benign	2	215386974	215386974	Human	2	name
150452008	CV1275122	single nucleotide variant	NM_212482.4(FN1):c.1675+21A>G	Glomerulopathy with fibronectin deposits 2 [RCV001703307]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001703308]\|not provided [RCV001713691]	benign	2	215420652	215420652	Human	2	name
150477285	CV1279421	single nucleotide variant	NM_212482.4(FN1):c.685+101T>C	not provided [RCV001714110]	benign	2	215430614	215430614	Human		name
150480886	CV1279604	single nucleotide variant	NM_212482.4(FN1):c.685+247A>C	not provided [RCV001714736]	benign	2	215430468	215430468	Human		name
150497524	CV1281409	duplication	NM_212482.4(FN1):c.277+280dup	not provided [RCV001717865]	benign	2	215434408	215434409	Human		name
150500784	CV1283843	single nucleotide variant	NM_212482.4(FN1):c.4895-99C>A	not provided [RCV001718465]	benign	2	215383582	215383582	Human		name
150500804	CV1283857	single nucleotide variant	NM_212482.4(FN1):c.7144+12C>G	not provided [RCV001718469]	benign	2	215365493	215365493	Human		name
150442142	CV1287676	single nucleotide variant	NM_212482.4(FN1):c.2713+38T>A	not provided [RCV001725396]	benign	2	215407089	215407089	Human		name
150551460	CV1292725	single nucleotide variant	NM_212482.4(FN1):c.6247+32G>A	not provided [RCV001754333]	benign	2	215373290	215373290	Human		name
150545298	CV1293103	single nucleotide variant	NM_212482.4(FN1):c.6714+31G>A	not provided [RCV001762889]	benign	2	215371878	215371878	Human		name
151235888	CV1319315	single nucleotide variant	NM_212482.4(FN1):c.278-229T>C	not provided [RCV001797260]	likely benign	2	215433690	215433690	Human		name
152138263	CV1525519	single nucleotide variant	NM_212482.4(FN1):c.5434+18C>A	not provided [RCV002137841]	likely benign	2	215380793	215380793	Human		name
152046352	CV1525830	single nucleotide variant	NM_212482.4(FN1):c.1216+13A>G	not provided [RCV002126687]	likely benign	2	215424133	215424133	Human		name
152175648	CV1527021	single nucleotide variant	NM_212482.4(FN1):c.6715-12C>G	not provided [RCV002163784]	likely benign	2	215370444	215370444	Human		name
152025794	CV1528016	single nucleotide variant	NM_212482.4(FN1):c.6853+13G>A	not provided [RCV002084583]	likely benign	2	215370281	215370281	Human		name
152038275	CV1530468	single nucleotide variant	NM_212482.4(FN1):c.4070-11T>C	Glomerulopathy with fibronectin deposits 2 [RCV005017106]\|not provided [RCV002087573]	likely benign	2	215391825	215391825	Human	1	name
152038449	CV1530515	single nucleotide variant	NM_212482.4(FN1):c.5623-18A>G	not provided [RCV002087596]	likely benign	2	215378280	215378280	Human		name
152036939	CV1532158	single nucleotide variant	NM_212482.4(FN1):c.3254-17T>C	not provided [RCV002125491]	likely benign	2	215399368	215399368	Human		name
152119908	CV1547302	single nucleotide variant	NM_212482.4(FN1):c.1216+19A>G	not provided [RCV002081410]	likely benign	2	215424127	215424127	Human		name
152125924	CV1548754	single nucleotide variant	NM_212482.4(FN1):c.7018+17T>C	not provided [RCV002082214]	likely benign	2	215367846	215367846	Human		name
152045111	CV1556061	single nucleotide variant	NM_212482.4(FN1):c.1394-12A>G	not provided [RCV002206837]	likely benign	2	215422255	215422255	Human		name
152061130	CV1558328	single nucleotide variant	NM_212482.4(FN1):c.7144+12C>T	not provided [RCV002128355]	likely benign	2	215365493	215365493	Human		name
152093746	CV1565607	single nucleotide variant	NM_212482.4(FN1):c.5164+14G>T	Glomerulopathy with fibronectin deposits 2 [RCV002494461]\|not provided [RCV002150923]	benign\|likely benign	2	215382198	215382198	Human	1	name
152029996	CV1568800	single nucleotide variant	NM_212482.4(FN1):c.7018+14T>C	not provided [RCV002186340]	likely benign	2	215367849	215367849	Human		name
152128224	CV1572216	single nucleotide variant	NM_212482.4(FN1):c.6157+20G>A	not provided [RCV002217704]	likely benign	2	215375194	215375194	Human		name
152064815	CV1576015	single nucleotide variant	NM_212482.4(FN1):c.2713+20A>G	Glomerulopathy with fibronectin deposits 2 [RCV002486824]\|not provided [RCV002209177]	likely benign	2	215407107	215407107	Human	1	name
152110735	CV1581694	single nucleotide variant	NM_212482.4(FN1):c.6158-13A>G	not provided [RCV002096813]	likely benign	2	215373424	215373424	Human		name
152157554	CV1586217	single nucleotide variant	NM_212482.4(FN1):c.3604+16A>G	not provided [RCV002140357]	likely benign	2	215397121	215397121	Human		name
152115124	CV1600463	single nucleotide variant	NM_212482.4(FN1):c.5164+15C>A	not provided [RCV002097374]	benign	2	215382197	215382197	Human		name
152159268	CV1605726	deletion	NM_212482.4(FN1):c.7363-20del	Glomerulopathy with fibronectin deposits 2 [RCV002486871]\|not provided [RCV002103482]	benign\|likely benign	2	215361646	215361646	Human	1	name
152027985	CV1607606	single nucleotide variant	NM_212482.4(FN1):c.7363-19C>T	not provided [RCV002105079]	benign	2	215361645	215361645	Human		name
152129574	CV1610317	single nucleotide variant	NM_212482.4(FN1):c.2122+10C>T	not provided [RCV002136758]	benign	2	215409924	215409924	Human		name
152063996	CV1612187	single nucleotide variant	NM_212482.4(FN1):c.2518+18C>A	not provided [RCV002128711]	likely benign	2	215408090	215408090	Human		name
152168961	CV1614014	single nucleotide variant	NM_212482.4(FN1):c.5622+12C>T	not provided [RCV002161289]	likely benign	2	215379118	215379118	Human		name
152032643	CV1614838	single nucleotide variant	NM_212482.4(FN1):c.1217-11G>A	Glomerulopathy with fibronectin deposits 2 [RCV002500129]\|not provided [RCV002086619]	likely benign	2	215423537	215423537	Human	1	name
152050040	CV1615238	single nucleotide variant	NM_212482.4(FN1):c.5164+15C>G	not provided [RCV002089037]	likely benign	2	215382197	215382197	Human		name
152146981	CV1615517	single nucleotide variant	NM_212482.4(FN1):c.1820-16A>G	Glomerulopathy with fibronectin deposits 2 [RCV002480980]\|not provided [RCV002101628]	likely benign	2	215414974	215414974	Human	1	name
152144867	CV1616368	single nucleotide variant	NM_212482.4(FN1):c.3349-10C>T	not provided [RCV002120877]	likely benign	2	215397858	215397858	Human		name
152111326	CV1617842	single nucleotide variant	NM_212482.4(FN1):c.4613-13C>T	not provided [RCV002116583]	likely benign	2	215384989	215384989	Human		name
152111005	CV1626048	single nucleotide variant	NM_212482.4(FN1):c.3605-18C>T	not provided [RCV002153053]	likely benign	2	215394737	215394737	Human		name
152157762	CV1630620	single nucleotide variant	NM_212482.4(FN1):c.5623-13C>G	Glomerulopathy with fibronectin deposits 2 [RCV002500013]\|not provided [RCV002122665]	benign\|likely benign	2	215378275	215378275	Human	1	name
152110491	CV1650919	single nucleotide variant	NM_212482.4(FN1):c.2299+16C>T	Glomerulopathy with fibronectin deposits 2 [RCV002494446]\|not provided [RCV002134418]	likely benign	2	215409547	215409547	Human	1	name
152110356	CV1665390	single nucleotide variant	NM_212482.4(FN1):c.1216+16G>A	not provided [RCV002080162]	likely benign	2	215424130	215424130	Human		name
156267748	CV1919037	single nucleotide variant	NM_133372.3(FNIP1):c.706+7G>C	not provided [RCV002627988]	likely benign	5	131710571	131710571	Human		name
156442267	CV1938493	single nucleotide variant	NM_133372.3(FNIP1):c.623-5T>C	not provided [RCV003112607]	likely benign	5	131710666	131710666	Human		name
156178658	CV1953311	single nucleotide variant	NM_212482.4(FN1):c.4894+14C>T	not provided [RCV002574044]	likely benign	2	215384006	215384006	Human		name
156211399	CV1955777	single nucleotide variant	NM_212482.4(FN1):c.2518+12G>A	not provided [RCV002575168]	likely benign	2	215408096	215408096	Human		name
156351810	CV1965498	deletion	NM_212482.4(FN1):c.1546+13del	not provided [RCV002581115]	likely benign	2	215422078	215422078	Human		name
156270904	CV1970939	single nucleotide variant	NM_212482.4(FN1):c.5710+17C>G	not provided [RCV002598087]	likely benign	2	215378158	215378158	Human		name
156067940	CV1975521	single nucleotide variant	NM_212482.4(FN1):c.1675+13A>G	not provided [RCV002591186]	likely benign	2	215420660	215420660	Human		name
155903809	CV1975848	single nucleotide variant	NM_212482.4(FN1):c.5434+13T>C	not provided [RCV002613550]	likely benign	2	215380798	215380798	Human		name
156131340	CV1977057	single nucleotide variant	NM_133372.3(FNIP1):c.219+3G>A	not provided [RCV002593506]	uncertain significance	5	131744561	131744561	Human		name
156094625	CV1980835	single nucleotide variant	NM_212482.4(FN1):c.4070-12G>A	not provided [RCV002621984]	likely benign	2	215391826	215391826	Human		name
156221780	CV1981342	single nucleotide variant	NM_133372.3(FNIP1):c.623-9G>A	not provided [RCV002626473]	likely benign	5	131710670	131710670	Human		name
156404360	CV1986343	single nucleotide variant	NM_212482.4(FN1):c.5887+11T>C	not provided [RCV002658033]	likely benign	2	215376487	215376487	Human		name
156337981	CV1988475	single nucleotide variant	NM_212482.4(FN1):c.5164+11A>G	not provided [RCV002631283]	benign	2	215382201	215382201	Human		name
156415323	CV1990959	single nucleotide variant	NM_212482.4(FN1):c.2713+13A>G	not provided [RCV002609614]	likely benign	2	215407114	215407114	Human		name
156341965	CV1998248	single nucleotide variant	NM_212482.4(FN1):c.6247+17G>A	not provided [RCV002650362]	likely benign	2	215373305	215373305	Human		name
156405916	CV2004519	single nucleotide variant	NM_212482.4(FN1):c.7252-10A>T	not provided [RCV002658429]	likely benign	2	215362089	215362089	Human		name
155956124	CV2014314	single nucleotide variant	NM_212482.4(FN1):c.5623-14C>T	not provided [RCV002686274]	likely benign	2	215378276	215378276	Human		name
156170464	CV2016116	single nucleotide variant	NM_212482.4(FN1):c.2986+15A>C	not provided [RCV002710469]	likely benign	2	215406223	215406223	Human		name
155910194	CV2027947	single nucleotide variant	NM_212482.4(FN1):c.4613-12T>G	not provided [RCV002726743]	likely benign	2	215384988	215384988	Human		name
156325216	CV2032437	single nucleotide variant	NM_212482.4(FN1):c.5622+13C>T	not provided [RCV002717366]	likely benign	2	215379117	215379117	Human		name
156224304	CV2037855	single nucleotide variant	NM_212482.4(FN1):c.7252-14C>G	not provided [RCV002790750]	likely benign	2	215362093	215362093	Human		name
155998218	CV2045389	single nucleotide variant	NM_212482.4(FN1):c.4729+15T>C	not provided [RCV002756072]	likely benign	2	215384845	215384845	Human		name
155999673	CV2045476	single nucleotide variant	NM_212482.4(FN1):c.4070-19C>A	not provided [RCV002756138]	likely benign	2	215391833	215391833	Human		name
156127604	CV2046994	single nucleotide variant	NM_212482.4(FN1):c.2986+15A>G	not provided [RCV002800485]	likely benign	2	215406223	215406223	Human		name
156215378	CV2047513	single nucleotide variant	NM_212482.4(FN1):c.6715-11G>A	not provided [RCV002790413]	likely benign	2	215370443	215370443	Human		name
156323124	CV2053878	single nucleotide variant	NM_212482.4(FN1):c.1037-15T>G	not provided [RCV002810212]	likely benign	2	215424340	215424340	Human		name
156181755	CV2068505	single nucleotide variant	NM_133372.3(FNIP1):c.92+12T>C	not provided [RCV002851856]	likely benign	5	131796818	131796818	Human		name
156147679	CV2078759	single nucleotide variant	NM_212482.4(FN1):c.5887+14T>C	not provided [RCV002872211]	likely benign	2	215376484	215376484	Human		name
155960921	CV2089006	single nucleotide variant	NM_133372.3(FNIP1):c.92+16G>T	not provided [RCV002881012]	likely benign	5	131796814	131796814	Human		name
156023587	CV2145471	single nucleotide variant	NM_212482.4(FN1):c.1941+11C>T	not provided [RCV003018347]	likely benign	2	215414826	215414826	Human		name
156355235	CV2165776	single nucleotide variant	NM_212482.4(FN1):c.2299+10A>T	not provided [RCV003031182]	likely benign	2	215409553	215409553	Human		name
156247931	CV2168790	single nucleotide variant	NM_212482.4(FN1):c.2987-20T>C	not provided [RCV003026239]	likely benign	2	215404675	215404675	Human		name
156136954	CV2177609	single nucleotide variant	NM_133372.3(FNIP1):c.531-6C>G	not provided [RCV003039902]	likely benign	5	131716662	131716662	Human		name
156353104	CV2190536	single nucleotide variant	NM_212482.4(FN1):c.4253-15C>A	not provided [RCV003048483]	likely benign	2	215388316	215388316	Human		name
156141527	CV2191921	deletion	NM_212482.4(FN1):c.1216+18del	not provided [RCV003056203]	benign	2	215424128	215424128	Human		name
405171462	CV2864312	single nucleotide variant	NM_212482.4(FN1):c.1819+12T>C	not provided [RCV003542199]	likely benign	2	215419230	215419230	Human		name
405067298	CV2875504	single nucleotide variant	NM_212482.4(FN1):c.5623-10A>T	not provided [RCV003548316]	likely benign	2	215378272	215378272	Human		name
402491517	CV2877714	single nucleotide variant	NM_212482.4(FN1):c.4894+17T>C	not provided [RCV003544990]	likely benign	2	215384003	215384003	Human		name
405239689	CV2882548	single nucleotide variant	NM_212482.4(FN1):c.4894+13A>C	not provided [RCV003557128]	likely benign	2	215384007	215384007	Human		name
405126236	CV2886622	single nucleotide variant	NM_212482.4(FN1):c.7145-14G>C	not provided [RCV003559596]	likely benign	2	215364999	215364999	Human		name
405152517	CV2888468	single nucleotide variant	NM_133372.3(FNIP1):c.456-7T>G	not provided [RCV003561723]	likely benign	5	131719067	131719067	Human		name
405176724	CV2951997	single nucleotide variant	NM_212482.4(FN1):c.7362+20A>G	not provided [RCV003675895]	likely benign	2	215361949	215361949	Human		name
405180000	CV2956176	single nucleotide variant	NM_133372.3(FNIP1):c.707-8A>C	not provided [RCV003676172]	likely benign	5	131709280	131709280	Human		name
405130202	CV2962345	single nucleotide variant	NM_133372.3(FNIP1):c.455+8G>C	not provided [RCV003668309]	likely benign	5	131719309	131719309	Human		name
405184409	CV2967572	single nucleotide variant	NM_212482.4(FN1):c.6158-18G>A	not provided [RCV003676608]	likely benign	2	215373429	215373429	Human		name
405199773	CV2982514	single nucleotide variant	NM_133372.3(FNIP1):c.531-8C>T	not provided [RCV003678068]	likely benign	5	131716664	131716664	Human		name
405202681	CV2989272	single nucleotide variant	NM_133372.3(FNIP1):c.707-5T>A	not provided [RCV003678343]	likely benign	5	131709277	131709277	Human		name
405120667	CV2994076	single nucleotide variant	NM_212482.4(FN1):c.2123-10G>C	not provided [RCV003723856]	likely benign	2	215409749	215409749	Human		name
402484936	CV3002124	single nucleotide variant	NM_212482.4(FN1):c.3349-20C>T	not provided [RCV003686964]	likely benign	2	215397868	215397868	Human		name
405032517	CV3009135	single nucleotide variant	NM_212482.4(FN1):c.3604+16A>C	not provided [RCV003695679]	likely benign	2	215397121	215397121	Human		name
404979198	CV3009503	single nucleotide variant	NM_212482.4(FN1):c.5050+20C>T	not provided [RCV003690941]	likely benign	2	215383308	215383308	Human		name
402524065	CV3011413	single nucleotide variant	NM_212482.4(FN1):c.3518-18A>C	not provided [RCV003716574]	likely benign	2	215397241	215397241	Human		name
405065166	CV3020820	single nucleotide variant	NM_212482.4(FN1):c.7145-19G>C	not provided [RCV003697973]	likely benign	2	215365004	215365004	Human		name
405180760	CV3027839	single nucleotide variant	NM_212482.4(FN1):c.2300-18T>C	not provided [RCV003705505]	likely benign	2	215408444	215408444	Human		name
405227074	CV3039429	single nucleotide variant	NM_212482.4(FN1):c.4895-15T>C	not provided [RCV003710811]	likely benign	2	215383498	215383498	Human		name
405253830	CV3044911	single nucleotide variant	NM_133372.3(FNIP1):c.707-4A>G	not provided [RCV003722642]	likely benign	5	131709276	131709276	Human		name
405244520	CV3054131	single nucleotide variant	NM_212482.4(FN1):c.5623-10A>G	not provided [RCV003719894]	likely benign	2	215378272	215378272	Human		name
405205414	CV3116997	single nucleotide variant	NM_212482.4(FN1):c.6715-12C>T	not provided [RCV003822481]	likely benign	2	215370444	215370444	Human		name
405009049	CV3118353	single nucleotide variant	NM_212482.4(FN1):c.2519-13C>T	not provided [RCV003828783]	likely benign	2	215407334	215407334	Human		name
405111867	CV3118537	single nucleotide variant	NM_212482.4(FN1):c.2123-17T>C	not provided [RCV003813765]	likely benign	2	215409756	215409756	Human		name
405005501	CV3120892	single nucleotide variant	NM_212482.4(FN1):c.2714-10T>C	Glomerulopathy with fibronectin deposits 2 [RCV005030287]\|not provided [RCV003828495]	likely benign	2	215406520	215406520	Human	1	name
404982115	CV3121456	single nucleotide variant	NM_212482.4(FN1):c.4252+16T>C	not provided [RCV003826255]	likely benign	2	215391616	215391616	Human		name
405088690	CV3122250	single nucleotide variant	NM_212482.4(FN1):c.1941+13C>T	not provided [RCV003811005]	likely benign	2	215414824	215414824	Human		name
405143837	CV3126107	single nucleotide variant	NM_212482.4(FN1):c.5164+10C>T	not provided [RCV003817023]	likely benign	2	215382202	215382202	Human		name
402523082	CV3127047	single nucleotide variant	NM_212482.4(FN1):c.1217-14A>G	not provided [RCV003824965]	likely benign	2	215423540	215423540	Human		name
405114672	CV3133823	single nucleotide variant	NM_133372.3(FNIP1):c.219+9C>A	not provided [RCV003836618]	likely benign	5	131744555	131744555	Human		name
405227589	CV3142852	single nucleotide variant	NM_212482.4(FN1):c.1394-17T>C	not provided [RCV003848195]	likely benign	2	215422260	215422260	Human		name
405174460	CV3148156	single nucleotide variant	NM_212482.4(FN1):c.3254-11C>G	not provided [RCV003858128]	likely benign	2	215399362	215399362	Human		name
405219683	CV3161471	single nucleotide variant	NM_212482.4(FN1):c.4729+19A>G	not provided [RCV003863340]	likely benign	2	215384841	215384841	Human		name
405201257	CV3164953	single nucleotide variant	NM_133372.3(FNIP1):c.456-4A>G	not provided [RCV003860814]	likely benign	5	131719064	131719064	Human		name
405197047	CV3168218	single nucleotide variant	NM_212482.4(FN1):c.3348+11G>C	not provided [RCV003860350]	likely benign	2	215399246	215399246	Human		name
402480918	CV3170744	single nucleotide variant	NM_212482.4(FN1):c.4343-19C>G	not provided [RCV003875946]	benign	2	215386977	215386977	Human		name
402524699	CV3175925	single nucleotide variant	NM_212482.4(FN1):c.2518+18C>G	not provided [RCV003880025]	likely benign	2	215408090	215408090	Human		name
402465895	CV3177373	single nucleotide variant	NM_133372.3(FNIP1):c.779-7T>C	not provided [RCV003873004]	likely benign	5	131706553	131706553	Human		name
405252067	CV3177468	single nucleotide variant	NM_212482.4(FN1):c.4343-16C>G	not provided [RCV003870426]	likely benign	2	215386974	215386974	Human		name
405252108	CV3177607	single nucleotide variant	NM_212482.4(FN1):c.4894+13A>G	not provided [RCV003870565]	likely benign	2	215384007	215384007	Human		name
402503457	CV3181069	single nucleotide variant	NM_212482.4(FN1):c.4343-20C>T	not provided [RCV003878086]	likely benign	2	215386978	215386978	Human		name
405271736	CV3202928	single nucleotide variant	NM_015308.5(FNBP4):c.450+8G>A	FNBP4-related disorder [RCV003913988]	likely benign	11	47754520	47754520	Human		name , trait , alternate_id
597634764	CV3709987	single nucleotide variant	NM_212482.4(FN1):c.6248-18C>T	Glomerulopathy with fibronectin deposits 2 [RCV005024003]\|not provided [RCV005063240]	likely benign\|uncertain significance	2	215372393	215372393	Human	1	name
597634800	CV3710003	single nucleotide variant	NM_212482.4(FN1):c.5435-10A>G	Glomerulopathy with fibronectin deposits 2 [RCV005024009]	uncertain significance	2	215379327	215379327	Human	1	name
597762535	CV3710030	single nucleotide variant	NM_212482.4(FN1):c.4612+20A>G	Glomerulopathy with fibronectin deposits 2 [RCV005018520]	uncertain significance	2	215386669	215386669	Human	1	name
597762590	CV3710051	single nucleotide variant	NM_212482.4(FN1):c.3797-12G>C	Glomerulopathy with fibronectin deposits 2 [RCV005018531]	uncertain significance	2	215393215	215393215	Human	1	name
597762611	CV3710057	single nucleotide variant	NM_212482.4(FN1):c.3518-17A>G	Glomerulopathy with fibronectin deposits 2 [RCV005018535]	uncertain significance	2	215397240	215397240	Human	1	name
597850592	CV3737251	duplication	NM_212482.4(FN1):c.7363-20dup	not provided [RCV005066217]	benign	2	215361645	215361646	Human		name
597887863	CV3739176	single nucleotide variant	NM_212482.4(FN1):c.1675+18C>T	not provided [RCV005070723]	likely benign	2	215420655	215420655	Human		name
597883011	CV3741236	single nucleotide variant	NM_212482.4(FN1):c.2713+19C>T	not provided [RCV005070143]	likely benign	2	215407108	215407108	Human		name
597853272	CV3743488	single nucleotide variant	NM_212482.4(FN1):c.7252-13T>C	not provided [RCV005060838]	likely benign	2	215362092	215362092	Human		name
597882702	CV3745058	single nucleotide variant	NM_212482.4(FN1):c.5051-18T>C	not provided [RCV005070083]	likely benign	2	215382343	215382343	Human		name
597959829	CV3746107	single nucleotide variant	NM_212482.4(FN1):c.2518+18C>T	not provided [RCV005081355]	likely benign	2	215408090	215408090	Human		name
597849111	CV3746666	single nucleotide variant	NM_212482.4(FN1):c.5164+17T>C	not provided [RCV005066063]	likely benign	2	215382195	215382195	Human		name
597849235	CV3746679	single nucleotide variant	NM_212482.4(FN1):c.7252-10A>C	not provided [RCV005066076]	likely benign	2	215362089	215362089	Human		name
597945415	CV3755363	single nucleotide variant	NM_212482.4(FN1):c.7363-12C>T	not provided [RCV005078372]	likely benign	2	215361638	215361638	Human		name
597951185	CV3756408	single nucleotide variant	NM_212482.4(FN1):c.2300-17T>G	not provided [RCV005079465]	likely benign	2	215408443	215408443	Human		name
597947725	CV3758978	single nucleotide variant	NM_212482.4(FN1):c.5622+11A>C	not provided [RCV005078774]	likely benign	2	215379119	215379119	Human		name
597962622	CV3791485	single nucleotide variant	NM_212482.4(FN1):c.4613-15C>G	not provided [RCV005139239]	likely benign	2	215384991	215384991	Human		name
597898454	CV3806951	single nucleotide variant	NM_212482.4(FN1):c.5710+16T>A	not provided [RCV005152338]	likely benign	2	215378159	215378159	Human		name
597934931	CV3807184	single nucleotide variant	NM_212482.4(FN1):c.3797-17G>T	not provided [RCV005157755]	likely benign	2	215393220	215393220	Human		name
597946183	CV3807300	single nucleotide variant	NM_133372.3(FNIP1):c.623-6A>T	not provided [RCV005159935]	likely benign	5	131710667	131710667	Human		name
597960363	CV3811865	single nucleotide variant	NM_212482.4(FN1):c.7252-15C>T	not provided [RCV005163518]	likely benign	2	215362094	215362094	Human		name
597856829	CV3816635	duplication	NM_212482.4(FN1):c.1216+11dup	not provided [RCV005146208]	likely benign	2	215424134	215424135	Human		name
597968646	CV3820996	single nucleotide variant	NM_133372.3(FNIP1):c.623-8C>G	not provided [RCV005165837]	likely benign	5	131710669	131710669	Human		name
597974279	CV3821068	single nucleotide variant	NM_212482.4(FN1):c.5711-11C>T	not provided [RCV005168389]	likely benign	2	215376685	215376685	Human		name
597858268	CV3822374	single nucleotide variant	NM_133372.3(FNIP1):c.354+9A>G	not provided [RCV005174672]	likely benign	5	131730895	131730895	Human		name
597858298	CV3822378	single nucleotide variant	NM_212482.4(FN1):c.3797-17G>C	not provided [RCV005174676]	likely benign	2	215393220	215393220	Human		name
597863709	CV3823039	single nucleotide variant	NM_212482.4(FN1):c.6157+14C>T	not provided [RCV005175389]	likely benign	2	215375200	215375200	Human		name
597875620	CV3829715	single nucleotide variant	NM_212482.4(FN1):c.5711-17G>A	not provided [RCV005177423]	likely benign	2	215376691	215376691	Human		name
597834588	CV3831927	single nucleotide variant	NM_212482.4(FN1):c.7019-17T>G	not provided [RCV005170930]	uncertain significance	2	215365647	215365647	Human		name
597975250	CV3832296	single nucleotide variant	NM_212482.4(FN1):c.5887+14T>A	not provided [RCV005169033]	likely benign	2	215376484	215376484	Human		name
597914482	CV3851112	single nucleotide variant	NM_212482.4(FN1):c.4612+13G>A	not provided [RCV005204080]	likely benign	2	215386676	215386676	Human		name
597905051	CV3853063	single nucleotide variant	NM_212482.4(FN1):c.5887+10C>T	not provided [RCV005202720]	likely benign	2	215376488	215376488	Human		name
597869321	CV3858420	single nucleotide variant	NM_212482.4(FN1):c.4729+17C>G	not provided [RCV005197163]	likely benign	2	215384843	215384843	Human		name
13612919	CV480689	single nucleotide variant	NM_133372.3(FNIP1):c.455+1G>A	Wolff-Parkinson-White pattern [RCV000656152]	uncertain significance	5	131719316	131719316	Human	1	name
15166381	CV730771	single nucleotide variant	NM_015308.5(FNBP4):c.451-9A>G	not provided [RCV000882620]	likely benign	11	47753111	47753111	Human		name
150333370	CV1170887	duplication	NM_212482.4(FN1):c.5623-259dup	not provided [RCV001539461]	benign	2	215378513	215378514	Human		name
150331632	CV1170888	duplication	NM_212482.4(FN1):c.5435-296dup	not provided [RCV001538712]	likely benign	2	215379603	215379604	Human		name
150337068	CV1170890	single nucleotide variant	NM_212482.4(FN1):c.1820-116A>G	not provided [RCV001541386]	likely benign	2	215415074	215415074	Human		name
150406882	CV1176091	single nucleotide variant	NM_212482.4(FN1):c.3605-261A>G	not provided [RCV001545402]	likely benign	2	215394980	215394980	Human		name
150422396	CV1179439	deletion	NM_212482.4(FN1):c.7362+107del	not provided [RCV001552577]	likely benign	2	215361862	215361862	Human		name
150420050	CV1179441	single nucleotide variant	NM_212482.4(FN1):c.4730-210G>A	not provided [RCV001551355]	likely benign	2	215384394	215384394	Human		name
150425172	CV1183099	single nucleotide variant	NM_212482.4(FN1):c.7144+197A>C	not provided [RCV001557655]	likely benign	2	215365308	215365308	Human		name
150424455	CV1183101	single nucleotide variant	NM_212482.4(FN1):c.7019-303C>T	not provided [RCV001556682]	likely benign	2	215365933	215365933	Human		name
150423260	CV1183102	single nucleotide variant	NM_212482.4(FN1):c.2714-198A>G	not provided [RCV001555081]	likely benign	2	215406708	215406708	Human		name
150423991	CV1183103	single nucleotide variant	NM_212482.4(FN1):c.1216+108C>T	not provided [RCV001556060]	likely benign	2	215424038	215424038	Human		name
150427047	CV1186376	deletion	NM_212482.4(FN1):c.7144+202del	not provided [RCV001560399]	likely benign	2	215365303	215365303	Human		name
150415557	CV1189802	single nucleotide variant	NM_212482.4(FN1):c.4729+201C>G	not provided [RCV001568037]	likely benign	2	215384659	215384659	Human		name
150405728	CV1193061	single nucleotide variant	NM_212482.4(FN1):c.4613-308C>T	not provided [RCV001571761]	likely benign	2	215385284	215385284	Human		name
150417562	CV1193064	single nucleotide variant	NM_212482.4(FN1):c.1217-231G>T	not provided [RCV001568820]	likely benign	2	215423757	215423757	Human		name
150419144	CV1196816	single nucleotide variant	NM_212482.4(FN1):c.7018+314T>C	not provided [RCV001577044]	likely benign	2	215367549	215367549	Human		name
150437277	CV1200955	single nucleotide variant	NM_212482.4(FN1):c.6854-314G>A	not provided [RCV001583035]	likely benign	2	215368341	215368341	Human		name
150439497	CV1201557	single nucleotide variant	NM_212482.4(FN1):c.4069+253C>T	not provided [RCV001583369]	likely benign	2	215392678	215392678	Human		name
150474848	CV1202158	single nucleotide variant	NM_212482.4(FN1):c.7019-150A>G	not provided [RCV001589401]	likely benign	2	215365780	215365780	Human		name
150430932	CV1204055	single nucleotide variant	NM_212482.4(FN1):c.5051-175G>C	not provided [RCV001580830]	likely benign	2	215382500	215382500	Human		name
150431025	CV1206212	single nucleotide variant	NM_212482.4(FN1):c.4612+133A>G	not provided [RCV001580860]	likely benign	2	215386556	215386556	Human		name
150431160	CV1206256	single nucleotide variant	NM_212482.4(FN1):c.6715-104T>G	not provided [RCV001580905]	likely benign	2	215370536	215370536	Human		name
150469816	CV1209212	single nucleotide variant	NM_212482.4(FN1):c.4894+215C>T	not provided [RCV001588323]	likely benign	2	215383805	215383805	Human		name
150470359	CV1209304	single nucleotide variant	NM_212482.4(FN1):c.5711-188T>A	not provided [RCV001588415]	likely benign	2	215376862	215376862	Human		name
150510468	CV1211709	single nucleotide variant	NM_212482.4(FN1):c.6714+150A>G	not provided [RCV001597604]	benign	2	215371759	215371759	Human		name
150504328	CV1212661	single nucleotide variant	NM_212482.4(FN1):c.1547-205G>A	not provided [RCV001595536]	benign	2	215421006	215421006	Human		name
150511438	CV1212745	single nucleotide variant	NM_212482.4(FN1):c.3605-146C>A	not provided [RCV001597977]	benign	2	215394865	215394865	Human		name
150511743	CV1212824	single nucleotide variant	NM_212482.4(FN1):c.6714+221A>G	not provided [RCV001598056]	benign	2	215371688	215371688	Human		name
150511932	CV1212873	single nucleotide variant	NM_212482.4(FN1):c.4252+128C>G	not provided [RCV001598105]	benign	2	215391504	215391504	Human		name
150514291	CV1213410	single nucleotide variant	NM_212482.4(FN1):c.6158-186T>C	not provided [RCV001599001]	benign	2	215373597	215373597	Human		name
150463915	CV1214852	single nucleotide variant	NM_212482.4(FN1):c.7019-181A>T	not provided [RCV001613848]	benign	2	215365811	215365811	Human		name
150464611	CV1215289	single nucleotide variant	NM_212482.4(FN1):c.3518-180G>A	not provided [RCV001613988]	benign	2	215397403	215397403	Human		name
150476514	CV1218487	single nucleotide variant	NM_212482.4(FN1):c.2713+175G>C	not provided [RCV001616114]	benign	2	215406952	215406952	Human		name
150497145	CV1219358	deletion	NM_212482.4(FN1):c.2518+160del	not provided [RCV001620027]	benign	2	215407948	215407948	Human		name
150497479	CV1219413	single nucleotide variant	NM_212482.4(FN1):c.7252-151C>T	not provided [RCV001620082]	benign	2	215362230	215362230	Human		name
150454508	CV1219998	single nucleotide variant	NM_212482.4(FN1):c.2987-262C>T	not provided [RCV001612380]	benign	2	215404917	215404917	Human		name
150455918	CV1220530	single nucleotide variant	NM_212482.4(FN1):c.4252+134A>C	not provided [RCV001612623]	benign	2	215391498	215391498	Human		name
150437941	CV1221093	single nucleotide variant	NM_212482.4(FN1):c.7251+201C>T	not provided [RCV001609787]	benign	2	215364678	215364678	Human		name
150436294	CV1221818	duplication	NM_212482.4(FN1):c.1675+295dup	not provided [RCV001609510]	benign	2	215420368	215420369	Human		name
150480739	CV1222028	single nucleotide variant	NM_212482.4(FN1):c.4070-170A>G	not provided [RCV001616825]	benign	2	215391984	215391984	Human		name
150497899	CV1224046	single nucleotide variant	NM_212482.4(FN1):c.5622+268A>G	not provided [RCV001620158]	benign	2	215378862	215378862	Human		name
150506203	CV1226288	single nucleotide variant	NM_212482.4(FN1):c.6853+298C>G	not provided [RCV001635656]	benign	2	215369996	215369996	Human		name
150516757	CV1227224	single nucleotide variant	NM_212482.4(FN1):c.3348+274C>T	not provided [RCV001639324]	benign	2	215398983	215398983	Human		name
150516335	CV1228312	single nucleotide variant	NM_212482.4(FN1):c.7019-180A>T	not provided [RCV001639118]	benign	2	215365810	215365810	Human		name
150513003	CV1228866	deletion	NM_212482.4(FN1):c.6714+235del	not provided [RCV001637708]	benign	2	215371674	215371674	Human		name
150513664	CV1229096	single nucleotide variant	NM_212482.4(FN1):c.5622+203T>C	not provided [RCV001637938]	benign	2	215378927	215378927	Human		name
150433223	CV1230452	single nucleotide variant	NM_212482.4(FN1):c.5164+277A>T	not provided [RCV001643397]	benign	2	215381935	215381935	Human	3	name
150453173	CV1231794	single nucleotide variant	NM_212482.4(FN1):c.5434+142G>A	not provided [RCV001648101]	benign	2	215380669	215380669	Human		name
150435817	CV1233964	single nucleotide variant	NM_212482.4(FN1):c.6715-115G>T	not provided [RCV001644091]	benign	2	215370547	215370547	Human		name
150474843	CV1234510	single nucleotide variant	NM_212482.4(FN1):c.3254-196C>A	not provided [RCV001651830]	benign	2	215399547	215399547	Human		name
150490600	CV1239144	single nucleotide variant	NM_212482.4(FN1):c.5888-143A>C	not provided [RCV001654712]	benign	2	215375861	215375861	Human		name
150491170	CV1239236	deletion	NM_212482.4(FN1):c.2518+161del	not provided [RCV001654804]	benign	2	215407947	215407947	Human		name
150503267	CV1241766	single nucleotide variant	NM_212482.4(FN1):c.1393+277G>C	not provided [RCV001657357]	benign	2	215423073	215423073	Human		name
150430934	CV1243528	single nucleotide variant	NM_212482.4(FN1):c.1394-310T>C	not provided [RCV001663147]	benign	2	215422553	215422553	Human		name
150434393	CV1243940	single nucleotide variant	NM_212482.4(FN1):c.6854-179C>T	not provided [RCV001665147]	likely benign	2	215368206	215368206	Human		name
150435525	CV1244434	single nucleotide variant	NM_212482.4(FN1):c.7144+195A>G	not provided [RCV001665425]	likely benign	2	215365310	215365310	Human		name
150507324	CV1244537	single nucleotide variant	NM_212482.4(FN1):c.7018+223A>G	not provided [RCV001658786]	likely benign	2	215367640	215367640	Human		name
150483615	CV1245140	single nucleotide variant	NM_212482.4(FN1):c.2714-277T>A	not provided [RCV001653317]	benign	2	215406787	215406787	Human		name
150441453	CV1246736	single nucleotide variant	NM_212482.4(FN1):c.6157+304C>G	not provided [RCV001666390]	benign	2	215374910	215374910	Human		name
150484877	CV1250114	single nucleotide variant	NM_212482.4(FN1):c.4894+137A>G	not provided [RCV001673727]	benign	2	215383883	215383883	Human		name
150485144	CV1250166	deletion	NM_212482.4(FN1):c.4613-273del	not provided [RCV001673779]	benign	2	215385249	215385249	Human		name
150446233	CV1250639	single nucleotide variant	NM_212482.4(FN1):c.6854-228G>T	not provided [RCV001667143]	benign	2	215368255	215368255	Human		name
150489716	CV1250907	deletion	NM_212482.4(FN1):c.3517+100del	not provided [RCV001674574]	benign	2	215397580	215397580	Human		name
150501885	CV1255135	single nucleotide variant	NM_212482.4(FN1):c.6854-198G>A	not provided [RCV001677054]	benign	2	215368225	215368225	Human		name
150505139	CV1255393	single nucleotide variant	NM_212482.4(FN1):c.7019-274G>A	not provided [RCV001677840]	benign	2	215365904	215365904	Human		name
150507727	CV1257210	single nucleotide variant	NM_212482.4(FN1):c.5050+169G>C	not provided [RCV001678509]	benign	2	215383159	215383159	Human		name
150506480	CV1257351	single nucleotide variant	NM_212482.4(FN1):c.3253+210G>A	not provided [RCV001678190]	benign	2	215404179	215404179	Human		name
150444410	CV1258515	single nucleotide variant	NM_212482.4(FN1):c.2713+206G>A	not provided [RCV001679713]	benign	2	215406921	215406921	Human		name
150470070	CV1259763	single nucleotide variant	NM_212482.4(FN1):c.4070-238T>C	not provided [RCV001684065]	benign	2	215392052	215392052	Human		name
150456724	CV1260046	single nucleotide variant	NM_212482.4(FN1):c.4894+221T>A	not provided [RCV001681526]	benign	2	215383799	215383799	Human		name
150448086	CV1261918	single nucleotide variant	NM_212482.4(FN1):c.4613-311G>A	not provided [RCV001680303]	benign	2	215385287	215385287	Human		name
150487917	CV1262811	duplication	NM_212482.4(FN1):c.6714+285dup	not provided [RCV001687209]	benign	2	215371610	215371611	Human		name
150484087	CV1263104	deletion	NM_212482.4(FN1):c.1676-177del	not provided [RCV001686504]	benign	2	215419562	215419562	Human		name
150460852	CV1264233	deletion	NM_212482.4(FN1):c.6714+298del	not provided [RCV001682150]	benign	2	215371611	215371611	Human		name
150438945	CV1264899	single nucleotide variant	NM_212482.4(FN1):c.6715-233T>C	not provided [RCV001678892]	benign	2	215370665	215370665	Human		name
150438992	CV1264907	single nucleotide variant	NM_212482.4(FN1):c.6247+116T>A	not provided [RCV001678900]	benign	2	215373206	215373206	Human		name
150439279	CV1264947	single nucleotide variant	NM_212482.4(FN1):c.4894+180G>A	not provided [RCV001678940]	benign	2	215383840	215383840	Human		name
150443636	CV1266422	single nucleotide variant	NM_212482.4(FN1):c.1941+287T>C	not provided [RCV001690858]	benign	2	215414550	215414550	Human		name
150438807	CV1266678	single nucleotide variant	NM_212482.4(FN1):c.4069+307G>T	not provided [RCV001690113]	benign	2	215392624	215392624	Human		name
150495073	CV1267460	single nucleotide variant	NM_212482.4(FN1):c.6714+100C>T	not provided [RCV001688488]	benign	2	215371809	215371809	Human		name
150491505	CV1267785	single nucleotide variant	NM_212482.4(FN1):c.2987-261G>A	not provided [RCV001687810]	benign	2	215404916	215404916	Human		name
150459940	CV1268416	single nucleotide variant	NM_212482.4(FN1):c.1394-131T>C	not provided [RCV001693413]	benign	2	215422374	215422374	Human		name
150457135	CV1269167	single nucleotide variant	NM_212482.4(FN1):c.1037-295C>T	not provided [RCV001692991]	benign	2	215424620	215424620	Human		name
150468161	CV1269352	single nucleotide variant	NM_212482.4(FN1):c.2518+161T>G	not provided [RCV001694760]	benign	2	215407947	215407947	Human		name
150499273	CV1270794	single nucleotide variant	NM_212482.4(FN1):c.7018+287G>T	not provided [RCV001689344]	benign	2	215367576	215367576	Human		name
150435832	CV1270865	deletion	NM_212482.4(FN1):c.7019-177del	not provided [RCV001689415]	benign	2	215365807	215365807	Human		name
150478888	CV1273373	single nucleotide variant	NM_212482.4(FN1):c.4895-254T>G	not provided [RCV001696576]	benign	2	215383737	215383737	Human		name
150449933	CV1275738	single nucleotide variant	NM_212482.4(FN1):c.7145-142G>A	not provided [RCV001708193]	benign	2	215365127	215365127	Human		name
150460667	CV1275854	single nucleotide variant	NM_212482.4(FN1):c.7144+147A>G	not provided [RCV001709792]	benign	2	215365358	215365358	Human		name
150463502	CV1276234	single nucleotide variant	NM_212482.4(FN1):c.1394-127T>C	not provided [RCV001710179]	benign	2	215422370	215422370	Human		name
150464440	CV1276391	single nucleotide variant	NM_212482.4(FN1):c.5165-277T>C	not provided [RCV001710336]	benign	2	215381357	215381357	Human		name
150450672	CV1276498	single nucleotide variant	NM_212482.4(FN1):c.4613-307G>A	not provided [RCV001708287]	benign	2	215385283	215385283	Human		name
150466418	CV1277402	single nucleotide variant	NM_212482.4(FN1):c.4252+204A>T	not provided [RCV001710697]	benign	2	215391428	215391428	Human		name
150467186	CV1277528	single nucleotide variant	NM_212482.4(FN1):c.2300-303C>T	not provided [RCV001710823]	benign	2	215408729	215408729	Human		name
150457874	CV1278688	single nucleotide variant	NM_212482.4(FN1):c.6157+178T>C	not provided [RCV001709304]	benign	2	215375036	215375036	Human		name
150474752	CV1278925	single nucleotide variant	NM_212482.4(FN1):c.1820-255T>A	not provided [RCV001713742]	benign	2	215415213	215415213	Human		name
150476846	CV1279339	duplication	NM_212482.4(FN1):c.1217-231dup	not provided [RCV001714048]	benign	2	215423749	215423750	Human		name
150483880	CV1280304	single nucleotide variant	NM_212482.4(FN1):c.6853+126C>T	not provided [RCV001715262]	benign	2	215370168	215370168	Human		name
150473431	CV1281480	single nucleotide variant	NM_212482.4(FN1):c.6715-122G>T	not provided [RCV001713529]	benign	2	215370554	215370554	Human		name
150487532	CV1283838	single nucleotide variant	NM_212482.4(FN1):c.4613-120G>A	not provided [RCV001715967]	benign	2	215385096	215385096	Human		name
150500768	CV1283840	single nucleotide variant	NM_212482.4(FN1):c.3797-325T>C	not provided [RCV001718462]	benign	2	215393528	215393528	Human		name
150487556	CV1283846	single nucleotide variant	NM_212482.4(FN1):c.4342+179A>G	not provided [RCV001715971]	benign	2	215388033	215388033	Human		name
150508678	CV1284342	single nucleotide variant	NM_212482.4(FN1):c.1820-325G>A	not provided [RCV001720450]	benign	2	215415283	215415283	Human		name
150441735	CV1287615	single nucleotide variant	NM_212482.4(FN1):c.3349-217T>C	not provided [RCV001725335]	benign	2	215398065	215398065	Human		name
151661178	CV1326867	single nucleotide variant	NM_133372.3(FNIP1):c.3306+1G>A	Immunodeficiency 93 and hypertrophic cardiomyopathy [RCV001822077]	pathogenic	5	131651801	131651801	Human	1	name
155268568	CV1704168	single nucleotide variant	NM_133372.3(FNIP1):c.3423-1G>T	not provided [RCV002284155]	not provided	5	131644764	131644764	Human		name
155268831	CV1705658	single nucleotide variant	NM_212482.4(FN1):c.4729+113C>T	not provided [RCV002286265]	likely benign	2	215384747	215384747	Human		name
156436779	CV1940355	single nucleotide variant	NM_133372.3(FNIP1):c.354+20T>G	not provided [RCV003106303]\|not specified [RCV003491315]	benign	5	131730884	131730884	Human		name
156443809	CV1941076	single nucleotide variant	NM_133372.3(FNIP1):c.1350-4T>C	not provided [RCV003114718]	likely benign	5	131677876	131677876	Human		name
156333244	CV1954254	single nucleotide variant	NM_133372.3(FNIP1):c.915-16A>G	not provided [RCV002580116]	likely benign	5	131704282	131704282	Human		name
156270188	CV1957153	single nucleotide variant	NM_133372.3(FNIP1):c.914+20A>G	not provided [RCV002577135]	likely benign	5	131706391	131706391	Human		name
156395205	CV1958861	single nucleotide variant	NM_133372.3(FNIP1):c.3109-5T>C	not provided [RCV002584299]	likely benign	5	131652004	131652004	Human		name
156407101	CV1963904	single nucleotide variant	NM_133372.3(FNIP1):c.915-13A>G	not provided [RCV002586121]	likely benign	5	131704279	131704279	Human		name
156392449	CV1965029	single nucleotide variant	NM_133372.3(FNIP1):c.219+14T>A	not provided [RCV002584000]	likely benign	5	131744550	131744550	Human		name
156247260	CV1988940	single nucleotide variant	NM_133372.3(FNIP1):c.1117-4C>T	not provided [RCV002627333]	likely benign	5	131699006	131699006	Human		name
155906418	CV2048193	single nucleotide variant	NM_133372.3(FNIP1):c.355-12G>T	not provided [RCV002771290]	benign	5	131719429	131719429	Human		name
156255694	CV2082796	single nucleotide variant	NM_133372.3(FNIP1):c.219+12T>C	not provided [RCV002877095]	likely benign	5	131744552	131744552	Human		name
156037322	CV2143272	single nucleotide variant	NM_133372.3(FNIP1):c.3306+8T>C	not provided [RCV002999384]	likely benign\|uncertain significance	5	131651794	131651794	Human		name
155948784	CV2164749	duplication	NM_133372.3(FNIP1):c.915-16dup	not provided [RCV003032314]	benign	5	131704281	131704282	Human		name
156097028	CV2310233	single nucleotide variant	NM_153756.3(FNDC5):c.633+40C>T	not specified [RCV004163332]	uncertain significance	1	32864624	32864624	Human		name
405224371	CV2885474	microsatellite	NM_212482.4(FN1):c.7252-8TC[2]	not provided [RCV003554404]	likely benign	2	215362082	215362083	Human		name
405174376	CV2919276	single nucleotide variant	NM_133372.3(FNIP1):c.1520-2A>G	not provided [RCV003563409]	likely pathogenic	5	131672926	131672926	Human		name
405113291	CV2939150	single nucleotide variant	NM_133372.3(FNIP1):c.456-18T>C	not provided [RCV003666597]	likely benign	5	131719078	131719078	Human		name
405136167	CV2958020	single nucleotide variant	NM_133372.3(FNIP1):c.3423-8T>C	not provided [RCV003672759]	likely benign	5	131644771	131644771	Human		name
405139692	CV2961860	single nucleotide variant	NM_133372.3(FNIP1):c.1202+7A>G	not provided [RCV003673117]	likely benign	5	131698910	131698910	Human		name
405162895	CV3017951	single nucleotide variant	NM_133372.3(FNIP1):c.707-14A>G	not provided [RCV003704091]	likely benign	5	131709286	131709286	Human		name
405123828	CV3021078	single nucleotide variant	NM_133372.3(FNIP1):c.1520-7A>G	not provided [RCV003701039]	likely benign	5	131672931	131672931	Human		name
402509429	CV3042398	single nucleotide variant	NM_133372.3(FNIP1):c.914+20A>T	not provided [RCV003715552]	likely benign	5	131706391	131706391	Human		name
405103794	CV3116262	single nucleotide variant	NM_133372.3(FNIP1):c.354+13A>G	not provided [RCV003811978]	likely benign	5	131730891	131730891	Human		name
404984228	CV3121694	single nucleotide variant	NM_133372.3(FNIP1):c.623-16C>T	not provided [RCV003826493]	likely benign	5	131710677	131710677	Human		name
405150439	CV3123221	single nucleotide variant	NM_133372.3(FNIP1):c.219+10A>G	not provided [RCV003817454]	likely benign	5	131744554	131744554	Human		name
405178080	CV3123527	single nucleotide variant	NM_133372.3(FNIP1):c.779-11T>C	not provided [RCV003819736]	likely benign	5	131706557	131706557	Human		name
405135120	CV3130514	single nucleotide variant	NM_133372.3(FNIP1):c.354+18A>C	not provided [RCV003838747]	likely benign	5	131730886	131730886	Human		name
405046911	CV3141708	single nucleotide variant	NM_133372.3(FNIP1):c.219+17A>G	not provided [RCV003831809]	likely benign	5	131744547	131744547	Human		name
405148999	CV3141994	single nucleotide variant	NM_133372.3(FNIP1):c.622+10T>C	not provided [RCV003839916]	likely benign	5	131716555	131716555	Human		name
405208220	CV3145668	single nucleotide variant	NM_133372.3(FNIP1):c.354+20T>A	not provided [RCV003845398]	likely benign	5	131730884	131730884	Human		name
405220238	CV3157735	single nucleotide variant	NM_133372.3(FNIP1):c.706+15G>A	not provided [RCV003863427]	likely benign	5	131710563	131710563	Human		name
405197000	CV3168213	single nucleotide variant	NM_133372.3(FNIP1):c.707-15C>T	not provided [RCV003860345]	likely benign	5	131709287	131709287	Human		name
402496199	CV3179210	single nucleotide variant	NM_133372.3(FNIP1):c.706+15G>T	not provided [RCV003877477]	likely benign	5	131710563	131710563	Human		name
597851972	CV3758523	single nucleotide variant	NM_133372.3(FNIP1):c.530+19A>G	not provided [RCV005088082]	likely benign	5	131718967	131718967	Human		name
597940041	CV3818774	deletion	NM_133372.3(FNIP1):c.1117-5del	not provided [RCV005158780]	benign	5	131699007	131699007	Human		name
597831355	CV3830753	single nucleotide variant	NM_133372.3(FNIP1):c.220-13T>C	not provided [RCV005170151]	likely benign	5	131731051	131731051	Human		name
598215513	CV3973590	single nucleotide variant	NM_153756.3(FNDC5):c.633+11G>C	not specified [RCV005339715]	uncertain significance	1	32864653	32864653	Human		name
15197140	CV730408	single nucleotide variant	NM_032532.3(FNDC1):c.1370-4G>A	not provided [RCV000889972]	benign	6	159231878	159231878	Human		name
15174915	CV779548	single nucleotide variant	NM_015308.5(FNBP4):c.906+10G>A	not provided [RCV000972823]	benign	11	47750906	47750906	Human		name
150334328	CV1170889	microsatellite	NM_212482.4(FN1):c.1942-38GT[9]	not provided [RCV001539984]	benign\|likely benign	2	215410131	215410134	Human		name
150516280	CV1228294	single nucleotide variant	NM_153756.3(FNDC5):c.499+250C>T	not provided [RCV001639100]	benign	1	32867503	32867503	Human		name
156436797	CV1940374	single nucleotide variant	NM_133372.3(FNIP1):c.3422+15T>C	not provided [RCV003106321]\|not specified [RCV003491316]	benign	5	131647075	131647075	Human		name
156438591	CV1947200	single nucleotide variant	NM_133372.3(FNIP1):c.1116+10G>A	not provided [RCV003108535]	likely benign	5	131704055	131704055	Human		name
156070815	CV1968720	single nucleotide variant	NM_133372.3(FNIP1):c.1117-18T>C	not provided [RCV002621238]	likely benign	5	131699020	131699020	Human		name
156412591	CV1968738	single nucleotide variant	NM_133372.3(FNIP1):c.1202+10G>A	not provided [RCV002608586]	likely benign	5	131698907	131698907	Human		name
156318110	CV1971377	single nucleotide variant	NM_133372.3(FNIP1):c.1519+19G>T	not provided [RCV002630177]	likely benign	5	131677684	131677684	Human		name
155918401	CV1981081	single nucleotide variant	NM_133372.3(FNIP1):c.3306+17C>T	not provided [RCV002614430]	likely benign	5	131651785	131651785	Human		name
156138499	CV2082170	single nucleotide variant	NM_133372.3(FNIP1):c.2940-16G>A	not provided [RCV002871897]	likely benign	5	131670647	131670647	Human		name
404982047	CV2848978	single nucleotide variant	NM_133372.3(FNIP1):c.2940-32A>T	not specified [RCV003488850]	benign	5	131670663	131670663	Human		name
404982011	CV2849006	single nucleotide variant	NM_133372.3(FNIP1):c.3108+74T>C	not specified [RCV003488878]	benign	5	131670389	131670389	Human		name
405116039	CV2951656	single nucleotide variant	NM_133372.3(FNIP1):c.3108+19T>C	not provided [RCV003670958]	likely benign	5	131670444	131670444	Human		name
405156934	CV2956565	deletion	NM_133372.3(FNIP1):c.2940-20del	not provided [RCV003674408]	benign	5	131670651	131670651	Human		name
405221421	CV2966166	single nucleotide variant	NM_133372.3(FNIP1):c.2940-15G>A	not provided [RCV003680745]	likely benign	5	131670646	131670646	Human		name
405219299	CV2968925	single nucleotide variant	NM_133372.3(FNIP1):c.1350-13A>C	not provided [RCV003680436]	likely benign	5	131677885	131677885	Human		name
405189435	CV2977877	single nucleotide variant	NM_133372.3(FNIP1):c.3307-14C>T	not provided [RCV003706258]	likely benign	5	131647219	131647219	Human		name
405004120	CV3120794	single nucleotide variant	NM_133372.3(FNIP1):c.3423-15T>C	not provided [RCV003828397]	likely benign	5	131644778	131644778	Human		name
405205831	CV3126680	single nucleotide variant	NM_133372.3(FNIP1):c.1203-18G>A	not provided [RCV003822614]	likely benign	5	131679193	131679193	Human		name
597888444	CV3739261	single nucleotide variant	NM_133372.3(FNIP1):c.1202+20C>G	not provided [RCV005070808]	likely benign	5	131698897	131698897	Human		name
597913774	CV3740526	single nucleotide variant	NM_133372.3(FNIP1):c.1116+10G>T	not provided [RCV005073863]	likely benign	5	131704055	131704055	Human		name
597832182	CV3751293	single nucleotide variant	NM_133372.3(FNIP1):c.1202+16C>T	not provided [RCV005084839]	likely benign	5	131698901	131698901	Human		name
597875720	CV3775865	single nucleotide variant	NM_133372.3(FNIP1):c.1202+18T>A	not provided [RCV005123392]	likely benign	5	131698899	131698899	Human		name
597838905	CV3824860	single nucleotide variant	NM_133372.3(FNIP1):c.2940-14C>T	not provided [RCV005171724]	likely benign	5	131670645	131670645	Human		name
597912164	CV3834226	single nucleotide variant	NM_133372.3(FNIP1):c.1203-20A>T	not provided [RCV005182988]	likely benign	5	131679195	131679195	Human		name
150509119	CV1214219	microsatellite	NM_212482.4(FN1):c.6248-327GA[2]	not provided [RCV001596740]	benign	2	215372697	215372698	Human		name
150500361	CV1224774	microsatellite	NM_212482.4(FN1):c.1942-38GT[10]	not provided [RCV001620606]	benign	2	215410131	215410132	Human		name
150510912	CV1242543	microsatellite	NM_212482.4(FN1):c.1942-38GT[12]	Glomerulopathy with fibronectin deposits 2 [RCV002501995]\|not provided [RCV001660895]	benign	2	215410130	215410131	Human		name
150446573	CV1261383	microsatellite	NM_212482.4(FN1):c.1942-38GT[13]	Glomerulopathy with fibronectin deposits 2 [RCV002496002]\|not provided [RCV001680057]	benign\|likely benign	2	215410130	215410131	Human		name
8651116	CV127691	single nucleotide variant	NM_015033.2(FNBP1):c.24+15616G>C	Lung cancer [RCV000108178]	uncertain significance	9	130027336	130027336	Human		name
152165740	CV1597258	microsatellite	NM_212482.4(FN1):c.1942-38GT[15]	not provided [RCV002124080]	likely benign	2	215410130	215410131	Human		name
152097792	CV1600026	microsatellite	NM_212482.4(FN1):c.1942-38GT[14]	Glomerulopathy with fibronectin deposits 2 [RCV002505821]\|not provided [RCV002151419]	benign\|likely benign	2	215410130	215410131	Human		name
15126993	CV778962	single nucleotide variant	NM_022763.4(FNDC3B):c.1971+10G>A	FNDC3B-related disorder [RCV003978412]\|not provided [RCV000963830]	benign	3	172341241	172341241	Human		name , alternate_id
150415083	CV1176093	microsatellite	NM_212482.4(FN1):c.1393+138TG[20]	not provided [RCV001548417]	likely benign	2	215423180	215423181	Human		name
150511265	CV1212688	microsatellite	NM_212482.4(FN1):c.1393+138TG[17]	not provided [RCV001597919]	benign	2	215423180	215423181	Human		name
150515583	CV1216256	microsatellite	NM_212482.4(FN1):c.2518+128TG[10]	not provided [RCV001608447]	benign	2	215407955	215407960	Human		name
150433617	CV1230585	microsatellite	NM_212482.4(FN1):c.3797-242AT[11]	not provided [RCV001643530]	benign	2	215393427	215393428	Human		name
150487757	CV1237384	microsatellite	NM_212482.4(FN1):c.1393+138TG[21]	not provided [RCV001654233]	benign	2	215423180	215423181	Human		name
150492492	CV1238186	microsatellite	NM_212482.4(FN1):c.2518+128TG[12]	not provided [RCV001655032]	benign	2	215407955	215407956	Human		name
150437090	CV1249813	microsatellite	NM_212482.4(FN1):c.1393+138TG[19]	not provided [RCV001665727]	benign	2	215423180	215423181	Human		name
150507564	CV1256965	microsatellite	NM_212482.4(FN1):c.1393+138TG[18]	not provided [RCV001678468]	benign	2	215423180	215423181	Human		name
150440964	CV1265485	microsatellite	NM_212482.4(FN1):c.1393+138TG[15]	not provided [RCV001679188]	benign	2	215423181	215423182	Human		name
150467340	CV1269214	microsatellite	NM_212482.4(FN1):c.3797-242AT[10]	not provided [RCV001694622]	benign	2	215393427	215393428	Human		name
150473468	CV1281495	microsatellite	NM_212482.4(FN1):c.2518+128TG[11]	not provided [RCV001713535]	benign	2	215407955	215407958	Human		name
401901902	CV2813900	single nucleotide variant	NM_001079673.2(FNDC3A):c.100-8T>C	not provided [RCV003393316]	likely benign	13	49075281	49075281	Human		name
405294868	CV3214940	single nucleotide variant	NM_001079673.2(FNDC3A):c.761-3A>T	FNDC3A-related disorder [RCV003936799]	likely benign	13	49138744	49138744	Human		name , trait , alternate_id
15176835	CV730037	single nucleotide variant	NM_001164473.3(FNBP1L):c.511-8G>T	not provided [RCV000884674]	benign	1	93530747	93530747	Human		name
8580366	CV114796	single nucleotide variant	NM_001008738.2(FNIP1):c.355-2666A>G	Lung cancer [RCV000095319]	uncertain significance	5	131722083	131722083	Human		name
150487245	CV1262707	duplication	NM_212482.4(FN1):c.149-27_149-25dup	not provided [RCV001687105]	benign	2	215434848	215434849	Human		name
151752136	CV1426827	deletion	NM_212482.4(FN1):c.5978-9_5978-8del	not provided [RCV002006969]	likely benign\|uncertain significance	2	215375401	215375402	Human		name
405095384	CV2874891	deletion	NM_212482.4(FN1):c.5888-4_5888-2del	not provided [RCV003550220]	uncertain significance	2	215375720	215375722	Human		name
15199840	CV760024	deletion	NM_015308.5(FNBP4):c.2009-2_2012del	not provided [RCV000912669]	likely benign	11	47724775	47724780	Human		name
150485812	CV1273910	microsatellite	NM_212482.4(FN1):c.1675+309GTTTTT[3]	not provided [RCV001698812]	benign	2	215420341	215420346	Human		name
152028670	CV1587099	microsatellite	NM_212482.4(FN1):c.6714+7_6714+10del	not provided [RCV002085540]	likely benign	2	215371899	215371902	Human		name
405143219	CV3056120	microsatellite	NM_212482.4(FN1):c.3605-13_3605-9del	not provided [RCV003725834]	likely benign	2	215394728	215394732	Human		name
405132845	CV3115252	deletion	NM_133372.3(FNIP1):c.220-10_220-9del	not provided [RCV003816097]	likely benign	5	131731047	131731048	Human		name
597918868	CV3842524	deletion	NM_212482.4(FN1):c.1217-11_1217-9del	not provided [RCV005184009]	likely benign	2	215423535	215423537	Human		name
15105327	CV759133	microsatellite	NM_212482.4(FN1):c.3517+8_3517+10del	not provided [RCV000915524]	likely benign	2	215397670	215397672	Human		name
127297912	CV1153979	deletion	NM_212482.4(FN1):c.2714-11_2714-10del	FN1-related disorder [RCV003940908]\|Glomerulopathy with fibronectin deposits 2 [RCV002501773]\|not provided [RCV001513052]	benign\|likely benign	2	215406520	215406521	Human	2	name , alternate_id
150413763	CV1189800	duplication	NM_212482.4(FN1):c.7362+97_7362+98dup	not provided [RCV001567305]	likely benign	2	215361861	215361862	Human		name
150451802	CV1220910	deletion	NM_212482.4(FN1):c.5978-12_5978-11del	not provided [RCV001612004]	benign	2	215375404	215375405	Human		name
150434986	CV1244087	microsatellite	NM_212482.4(FN1):c.6854-61_6854-59del	not provided [RCV001665294]	likely benign	2	215368086	215368088	Human		name
150487525	CV1283837	deletion	NM_212482.4(FN1):c.4894+34_4894+35del	not provided [RCV001715966]	benign	2	215383985	215383986	Human		name
156209869	CV2000887	deletion	NM_133372.3(FNIP1):c.914+13_914+19del	not provided [RCV002666803]	likely benign	5	131706392	131706398	Human		name
156039902	CV2049672	duplication	NM_212482.4(FN1):c.4894+10_4894+12dup	not provided [RCV002796394]	likely benign	2	215384007	215384008	Human		name
156268841	CV2102770	microsatellite	NM_133372.3(FNIP1):c.2940-6_2940-4del	not provided [RCV002895856]	benign	5	131670635	131670637	Human		name
405246980	CV2966530	microsatellite	NM_212482.4(FN1):c.2300-14_2300-10del	not provided [RCV003685557]	likely benign	2	215408436	215408440	Human		name
127299677	CV1153986	indel	NM_212482.4(FN1):c.149-4_149-3delinsTT	not provided [RCV001513804]	benign	2	215434827	215434828	Human		name
151880996	CV1395747	insertion	NM_212482.4(FN1):c.4613-11_4613-10insC	not provided [RCV002036877]	likely benign\|uncertain significance	2	215384986	215384987	Human		name
155794803	CV1859879	single nucleotide variant	NM_001202559.1(CHURC1-FNTB):c.465+8C>A	not specified [RCV002466123]	benign	14	65012397	65012397	Human		name
150335895	CV1164885	deletion	NM_212482.4(FN1):c.3518-180_3518-179del	not provided [RCV001530598]	benign	2	215397402	215397403	Human		name
150334744	CV1170886	deletion	NM_212482.4(FN1):c.6714+234_6714+235del	not provided [RCV001540215]	benign	2	215371674	215371675	Human		name
150425492	CV1183100	deletion	NM_212482.4(FN1):c.7019-180_7019-177del	not provided [RCV001558063]	likely benign	2	215365807	215365810	Human		name
150427690	CV1186377	deletion	NM_212482.4(FN1):c.4613-275_4613-273del	not provided [RCV001561266]	likely benign	2	215385249	215385251	Human		name
150477192	CV1218591	deletion	NM_212482.4(FN1):c.6158-265_6158-261del	not provided [RCV001616218]	benign	2	215373672	215373676	Human		name
150488294	CV1226035	deletion	NM_212482.4(FN1):c.4613-274_4613-273del	not provided [RCV001618196]	benign	2	215385249	215385250	Human		name
150517476	CV1226926	deletion	NM_212482.4(FN1):c.6158-275_6158-261del	not provided [RCV001640022]	benign	2	215373672	215373686	Human		name
150483441	CV1247621	deletion	NM_212482.4(FN1):c.1820-269_1820-268del	not provided [RCV001673447]	benign	2	215415226	215415227	Human		name
150475325	CV1251700	deletion	NM_212482.4(FN1):c.6715-122_6715-117del	not provided [RCV001671898]	benign	2	215370549	215370554	Human		name
150472555	CV1252264	deletion	NM_212482.4(FN1):c.1037-218_1037-215del	not provided [RCV001671465]	benign	2	215424540	215424543	Human		name
150462631	CV1253688	deletion	NM_212482.4(FN1):c.6158-274_6158-261del	not provided [RCV001669730]	benign	2	215373672	215373685	Human		name
150479979	CV1258344	microsatellite	NM_212482.4(FN1):c.5435-145_5435-142del	not provided [RCV001685763]	benign	2	215379459	215379462	Human		name
150484062	CV1263099	deletion	NM_212482.4(FN1):c.4613-276_4613-273del	not provided [RCV001686499]	benign	2	215385249	215385252	Human		name
150461760	CV1263271	microsatellite	NM_212482.4(FN1):c.1819+269_1819+270del	not provided [RCV001682268]	benign	2	215418972	215418973	Human		name
150467653	CV1269267	deletion	NM_212482.4(FN1):c.6714+233_6714+235del	not provided [RCV001694675]	benign	2	215371674	215371676	Human		name
150445538	CV1278169	deletion	NM_212482.4(FN1):c.7019-178_7019-177del	not provided [RCV001707312]	benign	2	215365807	215365808	Human		name
150487638	CV1283864	deletion	NM_212482.4(FN1):c.7019-179_7019-177del	not provided [RCV001715985]	benign	2	215365807	215365809	Human		name
401795735	CV2740214	single nucleotide variant	NM_001202559.1(CHURC1-FNTB):c.789-16G>A	not specified [RCV003320509]	likely benign	14	65032594	65032594	Human		name
150416301	CV1179440	insertion	NM_212482.4(FN1):c.7019-181_7019-180insT	not provided [RCV001549553]	likely benign	2	215365810	215365811	Human		name
150405659	CV1189801	insertion	NM_212482.4(FN1):c.7019-180_7019-179insT	not provided [RCV001564384]	likely benign	2	215365809	215365810	Human		name
150484086	CV1247065	insertion	NM_212482.4(FN1):c.1675+301_1675+302insG	not provided [RCV001673561]	benign	2	215420371	215420372	Human		name
150502005	CV1255173	insertion	NM_212482.4(FN1):c.3797-244_3797-243insT	not provided [RCV001677092]	benign	2	215393446	215393447	Human		name
150461158	CV1264272	insertion	NM_212482.4(FN1):c.3797-243_3797-242insT	not provided [RCV001682189]	benign	2	215393445	215393446	Human		name
156384030	CV1971681	insertion	NM_133372.3(FNIP1):c.1520-20_1520-19insT	not provided [RCV002604171]	likely benign	5	131672943	131672944	Human		name
150416877	CV1193063	insertion	NM_212482.4(FN1):c.3253+81_3253+82insCAAAA	not provided [RCV001568530]	likely benign	2	215404307	215404308	Human		name
156099482	CV2009655	indel	NM_212482.4(FN1):c.5622+20_5622+21delinsGG	not provided [RCV002706613]	likely benign	2	215379109	215379110	Human		name
597972923	CV3819997	indel	NM_212482.4(FN1):c.4253-16_4253-15delinsTG	not provided [RCV005167711]	uncertain significance	2	215388316	215388317	Human		name
150472407	CV1272483	insertion	NM_212482.4(FN1):c.3253+81_3253+82insCAAAAA	not provided [RCV001695539]	benign	2	215404307	215404308	Human		name
126741220	CV1019568	single nucleotide variant	NM_212482.4(FN1):c.3634C>G (p.Pro1212Ala)	FN1-related disorder [RCV005225386]\|Glomerulopathy with fibronectin deposits 2 [RCV001336197]	uncertain significance	2	215394690	215394690	Human	2	alternate_id
126750329	CV1024135	single nucleotide variant	NM_212482.4(FN1):c.3020A>G (p.Asn1007Ser)	FN1-related disorder [RCV004746339]\|Glomerulopathy with fibronectin deposits 2 [RCV002499705]\|not provided [RCV001352226]	uncertain significance	2	215404622	215404622	Human	2	alternate_id
127231922	CV1069018	single nucleotide variant	NM_212482.4(FN1):c.4857C>T (p.Pro1619=)	FN1-related disorder [RCV003908603]\|not provided [RCV001413254]	likely benign	2	215384057	215384057	Human	1	name , alternate_id
127257110	CV1090697	single nucleotide variant	NM_212482.4(FN1):c.3141T>C (p.Ser1047=)	FN1-related disorder [RCV003955954]\|not provided [RCV001437843]	likely benign	2	215404501	215404501	Human	1	name , alternate_id
127235080	CV1090698	single nucleotide variant	NM_212482.4(FN1):c.519A>G (p.Gly173=)	FN1-related disorder [RCV003965794]\|not provided [RCV001422197]	likely benign	2	215431861	215431861	Human	1	name , alternate_id
127318862	CV1153969	single nucleotide variant	NM_212482.4(FN1):c.6824G>A (p.Arg2275Gln)	FN1-related disorder [RCV003956208]\|not provided [RCV001521851]	benign	2	215370323	215370323	Human	1	alternate_id
127298226	CV1153975	single nucleotide variant	NM_212482.4(FN1):c.5274G>T (p.Ser1758=)	FN1-related disorder [RCV003921097]\|not provided [RCV001513179]	benign\|likely benign	2	215380971	215380971	Human	4	name , alternate_id
127298226	CV1153975	single nucleotide variant	NM_212482.4(FN1):c.5274G>T (p.Ser1758=)	FN1-related disorder [RCV003921097]\|not provided [RCV001513179]	benign\|likely benign	2	215380971	215380972	Human	4	name , alternate_id
127292272	CV1153983	single nucleotide variant	NM_212482.4(FN1):c.807G>A (p.Lys269=)	FN1-related disorder [RCV003908805]\|not provided [RCV001510793]	benign\|likely benign	2	215428217	215428217	Human	1	name , alternate_id
150545277	CV1293094	single nucleotide variant	NM_212482.4(FN1):c.5761A>T (p.Ile1921Phe)	FN1-related disorder [RCV003913360]\|Glomerulopathy with fibronectin deposits 2 [RCV002496066]\|not provided [RCV001762880]	benign\|likely benign	2	215376624	215376624	Human	2	alternate_id
151826920	CV1392354	single nucleotide variant	NM_212482.4(FN1):c.352T>G (p.Ser118Ala)	FN1-related disorder [RCV003892910]\|Inborn genetic diseases [RCV005330958]\|not provided [RCV001879742]	likely benign\|uncertain significance	2	215433387	215433387	Human	2	name , alternate_id
151879637	CV1395638	single nucleotide variant	NM_212482.4(FN1):c.2717C>T (p.Thr906Ile)	FN1-related disorder [RCV004746573]\|Glomerulopathy with fibronectin deposits 2 [RCV002486614]\|Inborn genetic diseases [RCV002642068]\|not provided [RCV001999366]	likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	215406507	215406507	Human	3	alternate_id
151892427	CV1481069	single nucleotide variant	NM_212482.4(FN1):c.6047C>T (p.Pro2016Leu)	FN1-related disorder [RCV003407973]\|not provided [RCV001944101]	likely benign\|uncertain significance	2	215375324	215375324	Human	1	alternate_id
152106571	CV1527395	single nucleotide variant	NM_212482.4(FN1):c.7295G>C (p.Ser2432Thr)	FN1-related disorder [RCV003913778]\|not provided [RCV002079687]	benign\|likely benign	2	215362036	215362036	Human	1	alternate_id
152129107	CV1546289	single nucleotide variant	NM_212482.4(FN1):c.1002G>A (p.Thr334=)	FN1-related disorder [RCV003923662]\|Glomerulopathy with fibronectin deposits 2 [RCV002494287]\|not provided [RCV002136702]	benign\|likely benign	2	215425128	215425128	Human	2	name , alternate_id
152027182	CV1562532	single nucleotide variant	NM_212482.4(FN1):c.3804C>T (p.Pro1268=)	FN1-related disorder [RCV003903330]\|not provided [RCV002104807]	likely benign	2	215393196	215393196	Human	1	name , alternate_id
152124677	CV1587453	single nucleotide variant	NM_212482.4(FN1):c.1782T>C (p.Ile594=)	FN1-related disorder [RCV003971090]\|not provided [RCV002136163]	benign\|likely benign	2	215419279	215419279	Human	1	name , alternate_id
152043305	CV1618190	single nucleotide variant	NM_212482.4(FN1):c.2805C>T (p.Thr935=)	FN1-related disorder [RCV003960937]\|not provided [RCV002206628]	likely benign	2	215406419	215406419	Human	1	name , alternate_id
152151514	CV1631439	single nucleotide variant	NM_212482.4(FN1):c.4257C>T (p.Leu1419=)	FN1-related disorder [RCV003923463]\|not provided [RCV002179521]	benign\|likely benign	2	215388297	215388297	Human	1	alternate_id
156144525	CV1922833	single nucleotide variant	NM_212482.4(FN1):c.4175G>A (p.Arg1392His)	FN1-related disorder [RCV003963701]\|Glomerulopathy with fibronectin deposits 2 [RCV005028284]\|Inborn genetic diseases [RCV002623782]\|not provided [RCV002607638]	uncertain significance	2	215391709	215391709	Human	3	alternate_id
401905385	CV2796225	single nucleotide variant	NM_212482.4(FN1):c.6175G>A (p.Glu2059Lys)	FN1-related disorder [RCV003420830]\|Glomerulopathy with fibronectin deposits 2 [RCV005030012]\|not provided [RCV005061380]	likely benign\|uncertain significance	2	215373394	215373394	Human	2	alternate_id
401937655	CV2798873	indel	NM_212482.4(FN1):c.4448_4449delinsGC (p.His1483Arg)	FN1-related disorder [RCV003416712]	uncertain significance	2	215386852	215386853	Human		trait , alternate_id
401931884	CV2798951	single nucleotide variant	NM_212482.4(FN1):c.1503T>G (p.Asn501Lys)	FN1-related disorder [RCV003391626]	uncertain significance	2	215422134	215422134	Human		trait , alternate_id
401913731	CV2799080	single nucleotide variant	NM_212482.4(FN1):c.2235C>A (p.Asp745Glu)	FN1-related disorder [RCV003400237]\|not provided [RCV005062895]	uncertain significance	2	215409627	215409627	Human	1	alternate_id
401913698	CV2799610	single nucleotide variant	NM_212482.4(FN1):c.1261C>T (p.His421Tyr)	FN1-related disorder [RCV003427940]	uncertain significance	2	215423482	215423482	Human		trait , alternate_id
401923718	CV2803373	single nucleotide variant	NM_212482.4(FN1):c.3216C>A (p.Asn1072Lys)	FN1-related disorder [RCV003404519]	uncertain significance	2	215404426	215404426	Human		trait , alternate_id
401931605	CV2803623	single nucleotide variant	NM_212482.4(FN1):c.6686C>T (p.Pro2229Leu)	FN1-related disorder [RCV003391454]\|Inborn genetic diseases [RCV005335762]\|not provided [RCV004696535]	uncertain significance	2	215371937	215371937	Human	2	alternate_id
401901770	CV2804687	single nucleotide variant	NM_212482.4(FN1):c.4452T>A (p.His1484Gln)	FN1-related disorder [RCV003393204]\|Inborn genetic diseases [RCV004978852]	uncertain significance	2	215386849	215386849	Human	2	alternate_id
402464825	CV2916471	indel	NM_212482.4(FN1):c.6456_6458delinsTTATGCCTAAAGTGGTTTTAG (p.Pro2153delinsTyrAlaTer)	FN1-related disorder [RCV003909051]\|not provided [RCV003569104]	uncertain significance	2	215372165	215372167	Human		alternate_id
8565563	CV31364	single nucleotide variant	NM_212482.4(FN1):c.2918A>G (p.Tyr973Cys)	FN1-related disorder [RCV004745163]\|Glomerulopathy with fibronectin deposits 2 [RCV000017722]\|Glomerulopathy with fibronectin deposits 2 [RCV002482881]\|not provided [RCV005089267]	pathogenic\|uncertain significance	2	215406306	215406306	Human	2	alternate_id
405241644	CV3176909	single nucleotide variant	NM_212482.4(FN1):c.4826T>G (p.Val1609Gly)	FN1-related disorder [RCV003939245]\|not provided [RCV003867347]	uncertain significance	2	215384088	215384088	Human	1	alternate_id
405291612	CV3205868	single nucleotide variant	NM_212482.4(FN1):c.4449T>C (p.His1483=)	FN1-related disorder [RCV003963987]	likely benign	2	215386852	215386852	Human		trait , alternate_id
405274404	CV3208772	single nucleotide variant	NM_212482.4(FN1):c.6321A>C (p.Thr2107=)	FN1-related disorder [RCV003951581]\|Glomerulopathy with fibronectin deposits 2 [RCV005030364]\|not provided [RCV005101838]	likely benign\|uncertain significance	2	215372302	215372302	Human	2	alternate_id
405294462	CV3211345	single nucleotide variant	NM_212482.4(FN1):c.808T>C (p.Cys270Arg)	FN1-related disorder [RCV003934359]	uncertain significance	2	215428216	215428216	Human		trait , alternate_id
405279504	CV3217425	single nucleotide variant	NM_212482.4(FN1):c.6282C>T (p.Pro2094=)	FN1-related disorder [RCV003976844]	likely benign	2	215372341	215372341	Human		trait , alternate_id
405271013	CV3218888	single nucleotide variant	NM_212482.4(FN1):c.2451G>A (p.Thr817=)	FN1-related disorder [RCV003971634]	likely benign	2	215408175	215408175	Human		name , trait , alternate_id
408376758	CV3505691	single nucleotide variant	NM_212482.4(FN1):c.4311G>C (p.Glu1437Asp)	FN1-related disorder [RCV004726647]	uncertain significance	2	215388243	215388243	Human		trait , alternate_id
408375182	CV3510586	single nucleotide variant	NM_212482.4(FN1):c.6721G>A (p.Val2241Ile)	FN1-related disorder [RCV004747869]\|Glomerulopathy with fibronectin deposits 2 [RCV005023672]\|not provided [RCV005103744]	likely benign\|uncertain significance	2	215370426	215370426	Human	2	alternate_id
408375235	CV3510944	single nucleotide variant	NM_212482.4(FN1):c.2158C>T (p.Pro720Ser)	FN1-related disorder [RCV004747919]	uncertain significance	2	215409704	215409704	Human		trait , alternate_id
408375302	CV3511333	single nucleotide variant	NM_212482.4(FN1):c.301T>A (p.Tyr101Asn)	FN1-related disorder [RCV004747983]\|Inborn genetic diseases [RCV005335990]\|not provided [RCV005103763]	uncertain significance	2	215433438	215433438	Human	2	alternate_id
408373931	CV3513315	single nucleotide variant	NM_212482.4(FN1):c.7259G>A (p.Arg2420His)	FN1-related disorder [RCV004745825]\|not provided [RCV005059856]	uncertain significance	2	215362072	215362072	Human	1	alternate_id
15113730	CV719594	single nucleotide variant	NM_212482.4(FN1):c.3307A>C (p.Ile1103Leu)	FN1-related disorder [RCV003922836]\|not provided [RCV000894719]	benign	2	215399298	215399298	Human	1	alternate_id
15195856	CV719595	single nucleotide variant	NM_212482.4(FN1):c.2808C>G (p.Gly936=)	FN1-related disorder [RCV004746132]\|not provided [RCV000889620]	benign	2	215406416	215406416	Human	1	name , alternate_id
15108768	CV719597	single nucleotide variant	NM_212482.4(FN1):c.1860G>A (p.Pro620=)	FN1-related disorder [RCV003940747]\|Glomerulopathy with fibronectin deposits 2 [RCV002487957]\|not provided [RCV000893732]	likely benign	2	215414918	215414918	Human	2	name , alternate_id
15175549	CV719601	single nucleotide variant	NM_212482.4(FN1):c.202A>T (p.Thr68Ser)	FN1-related disorder [RCV003948348]\|not provided [RCV000884393]	likely benign	2	215434771	215434771	Human	1	name , alternate_id
15140592	CV733145	single nucleotide variant	NM_212482.4(FN1):c.5532A>C (p.Arg1844=)	FN1-related disorder [RCV003912839]\|Glomerulopathy with fibronectin deposits 2 [RCV002495442]\|not provided [RCV000899346]	benign\|likely benign	2	215379220	215379220	Human	2	name , alternate_id
15165451	CV733151	single nucleotide variant	NM_212482.4(FN1):c.751A>T (p.Asn251Tyr)	FN1-related disorder [RCV003932879]\|not provided [RCV000904223]	benign\|likely benign	2	215428273	215428273	Human	1	name , alternate_id
15168064	CV747275	single nucleotide variant	NM_212482.4(FN1):c.2144C>T (p.Thr715Met)	FN1-related disorder [RCV003960455]\|not provided [RCV000927216]	benign\|likely benign	2	215409718	215409718	Human	1	alternate_id
15194616	CV747279	single nucleotide variant	NM_212482.4(FN1):c.1361C>A (p.Ala454Asp)	FN1-related disorder [RCV004746152]\|Glomerulopathy with fibronectin deposits 2 [RCV005392540]\|Inborn genetic diseases [RCV003169284]\|not provided [RCV000911176]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	2	215423382	215423382	Human	3	alternate_id
15181337	CV762890	single nucleotide variant	NM_212482.4(FN1):c.1626C>T (p.Asn542=)	FN1-related disorder [RCV004746165]\|Glomerulopathy with fibronectin deposits 2 [RCV002505381]\|not provided [RCV000930102]	benign\|likely benign	2	215420722	215420722	Human	2	name , alternate_id
126748069	CV988355	single nucleotide variant	NM_212482.4(FN1):c.3062G>A (p.Arg1021Gln)	FN1-related disorder [RCV003399081]\|not provided [RCV001306363]	uncertain significance	2	215404580	215404580	Human	1	alternate_id
126755366	CV988356	single nucleotide variant	NM_212482.4(FN1):c.2429C>T (p.Ala810Val)	FN1-related disorder [RCV003416181]\|Glomerulopathy with fibronectin deposits 2 [RCV002476420]\|not provided [RCV001307844]	uncertain significance	2	215408197	215408197	Human	2	alternate_id
150408193	CV1199931	single nucleotide variant	NM_133372.3(FNIP1):c.1553G>A (p.Arg518Gln)	FNIP1-related disorder [RCV003910907]\|not provided [RCV001580059]	benign\|likely benign\|conflicting interpretations of pathogenicity\|uncertain significance	5	131672891	131672891	Human	4	alternate_id
401902850	CV2799688	single nucleotide variant	NM_133372.3(FNIP1):c.2210T>C (p.Ile737Thr)	FNIP1-related disorder [RCV003419099]	uncertain significance	5	131672234	131672234	Human		trait , alternate_id
408383865	CV3505934	microsatellite	NM_015308.5(FNBP4):c.1894GAA[3] (p.Glu635del)	FNBP4-related disorder [RCV004731344]	uncertain significance	11	47731477	47731479	Human		trait , alternate_id
408367257	CV3508073	single nucleotide variant	NM_015308.5(FNBP4):c.1409G>A (p.Arg470Lys)	FNBP4-related disorder [RCV004758317]	uncertain significance	11	47744000	47744000	Human		trait , alternate_id
401927585	CV2825063	single nucleotide variant	NM_022763.4(FNDC3B):c.1698G>A (p.Thr566=)	FNDC3B-related disorder [RCV003938992]\|not provided [RCV003439054]	likely benign	3	172335000	172335000	Human		alternate_id
405276287	CV3193325	single nucleotide variant	NM_022763.4(FNDC3B):c.1374T>C (p.Gly458=)	FNDC3B-related disorder [RCV003974492]	benign	3	172329071	172329071	Human	3	trait , alternate_id
405276896	CV3193523	single nucleotide variant	NM_001079673.2(FNDC3A):c.3049A>G (p.Thr1017Ala)	FNDC3A-related disorder [RCV003974691]	benign	13	49201861	49201861	Human		trait , alternate_id
405275849	CV3199511	single nucleotide variant	NM_001079673.2(FNDC3A):c.3132A>G (p.Lys1044=)	FNDC3A-related disorder [RCV003916910]	benign	13	49201944	49201944	Human		trait , alternate_id
405274948	CV3199863	single nucleotide variant	NM_022763.4(FNDC3B):c.687T>C (p.His229=)	FNDC3B-related disorder [RCV003973899]	benign	3	172251438	172251438	Human		trait , alternate_id
405280118	CV3200258	single nucleotide variant	NM_001079673.2(FNDC3A):c.2589C>T (p.Ser863=)	FNDC3A-related disorder [RCV003977169]	likely benign	13	49198080	49198080	Human		trait , alternate_id
405280347	CV3200718	single nucleotide variant	NM_022763.4(FNDC3B):c.536C>G (p.Thr179Ser)	FNDC3B-related disorder [RCV003977343]	benign	3	172251287	172251287	Human	11	trait , alternate_id
405258269	CV3203189	single nucleotide variant	NM_022763.4(FNDC3B):c.2590G>A (p.Val864Ile)	FNDC3B-related disorder [RCV003941796]	benign	3	172352878	172352878	Human		trait , alternate_id
405258453	CV3203815	single nucleotide variant	NM_001079673.2(FNDC3A):c.2043A>G (p.Leu681=)	FNDC3A-related disorder [RCV003941986]	likely benign	13	49191113	49191113	Human		trait , alternate_id
405292849	CV3210407	single nucleotide variant	NM_022763.4(FNDC3B):c.1354G>T (p.Ala452Ser)	FNDC3B-related disorder [RCV003931376]	benign	3	172329051	172329051	Human		trait , alternate_id
405255852	CV3211324	single nucleotide variant	NM_022763.4(FNDC3B):c.771G>C (p.Ser257=)	FNDC3B-related disorder [RCV003939426]	benign	3	172251522	172251522	Human		trait , alternate_id
405284187	CV3213632	single nucleotide variant	NM_022763.4(FNDC3B):c.2511A>G (p.Leu837=)	FNDC3B-related disorder [RCV003922202]	likely benign	3	172347358	172347358	Human		trait , alternate_id
405294197	CV3214637	single nucleotide variant	NM_001079673.2(FNDC3A):c.1653A>G (p.Pro551=)	FNDC3A-related disorder [RCV003934080]	likely benign	13	49185999	49185999	Human		trait , alternate_id
405270155	CV3215436	single nucleotide variant	NM_022763.4(FNDC3B):c.2568G>T (p.Thr856=)	FNDC3B-related disorder [RCV003949182]	likely benign	3	172352856	172352856	Human		trait , alternate_id
405294685	CV3215587	single nucleotide variant	NM_001079673.2(FNDC3A):c.1221A>G (p.Glu407=)	FNDC3A-related disorder [RCV003934605]	likely benign	13	49172087	49172087	Human		trait , alternate_id
15187206	CV697931	single nucleotide variant	NM_022763.4(FNDC3B):c.1137C>T (p.Pro379=)	FNDC3B-related disorder [RCV003915830]\|not provided [RCV000953518]	benign	3	172307438	172307438	Human		alternate_id
15119003	CV713949	single nucleotide variant	NM_001079673.2(FNDC3A):c.1752C>T (p.Thr584=)	FNDC3A-related disorder [RCV003916079]\|not provided [RCV000962477]	benign	13	49186098	49186098	Human		alternate_id
15098417	CV720303	single nucleotide variant	NM_022763.4(FNDC3B):c.2967G>C (p.Glu989Asp)	FNDC3B-related disorder [RCV003930809]\|not provided [RCV000891729]	benign	3	172362804	172362804	Human		alternate_id
151663028	CV1333652	single nucleotide variant	NM_212482.4(FN1):c.833C>G (p.Thr278Ser)	X-linked Alport syndrome [RCV001838830]\|not provided [RCV001869848]	uncertain significance	2	215428191	215428191	Human	1	name , alternate_id
156120587	CV2013759	single nucleotide variant	NM_212482.4(FN1):c.9G>C (p.Arg3Ser)	Glomerulopathy with fibronectin deposits 2 [RCV005019346]\|not provided [RCV002740181]	uncertain significance	2	215435794	215435794	Human	1	name
402490341	CV2867141	single nucleotide variant	NM_212482.4(FN1):c.4C>T (p.Leu2Phe)	not provided [RCV003544883]	uncertain significance	2	215435799	215435799	Human		name
405079199	CV2945440	single nucleotide variant	NM_212482.4(FN1):c.72G>A (p.Thr24=)	not provided [RCV003664458]	likely benign	2	215435731	215435731	Human		name
405075494	CV3007855	single nucleotide variant	NM_212482.4(FN1):c.63G>A (p.Val21=)	not provided [RCV003716732]	likely benign	2	215435740	215435740	Human		name
15201442	CV719603	single nucleotide variant	NM_212482.4(FN1):c.54G>C (p.Gly18=)	not provided [RCV000891194]	benign\|likely benign	2	215435749	215435749	Human		name
127273223	CV1090700	single nucleotide variant	NM_212482.4(FN1):c.219G>T (p.Ala73=)	not provided [RCV001442458]	likely benign	2	215434754	215434754	Human		name
152113956	CV1574611	single nucleotide variant	NM_212482.4(FN1):c.247C>A (p.Arg83=)	Glomerulopathy with fibronectin deposits 2 [RCV002499939]\|not provided [RCV002116931]	likely benign	2	215434726	215434726	Human	1	name
155947654	CV2036057	single nucleotide variant	NM_212482.4(FN1):c.147G>A (p.Lys49=)	not provided [RCV002775585]	uncertain significance	2	215435656	215435656	Human		name
155922131	CV2102466	variation	NM_133372.3(FNIP1):c.226= (p.Gly76=)	not provided [RCV002903404]	benign	5	131731032	131731032	Human		name
156218928	CV2128137	single nucleotide variant	NM_212482.4(FN1):c.14C>T (p.Pro5Leu)	not provided [RCV002958061]	uncertain significance	2	215435789	215435789	Human		name
156277855	CV2328349	single nucleotide variant	NM_022158.4(FN3K):c.7C>G (p.Gln3Glu)	not specified [RCV004175465]	uncertain significance	17	82735643	82735643	Human		name
405217117	CV2897289	single nucleotide variant	NM_212482.4(FN1):c.222G>A (p.Leu74=)	not provided [RCV003567922]	likely benign	2	215434751	215434751	Human		name
405152722	CV2949236	single nucleotide variant	NM_212482.4(FN1):c.201G>T (p.Arg67=)	not provided [RCV003674124]	likely benign	2	215434772	215434772	Human		name
405187549	CV2964214	single nucleotide variant	NM_212482.4(FN1):c.19C>T (p.Pro7Ser)	not provided [RCV003676896]	uncertain significance	2	215435784	215435784	Human		name
405193383	CV2984830	single nucleotide variant	NM_212482.4(FN1):c.231T>C (p.Thr77=)	not provided [RCV003706502]	likely benign	2	215434742	215434742	Human		name
402502804	CV3007010	variation	NM_212482.4(FN1):c.2449= (p.Thr817=)	not provided [RCV003688675]	uncertain significance	2	215408177	215408177	Human		name
405204667	CV3033537	single nucleotide variant	NM_212482.4(FN1):c.25C>A (p.Leu9Met)	not provided [RCV003707848]	uncertain significance	2	215435778	215435778	Human		name
405227131	CV3039579	single nucleotide variant	NM_212482.4(FN1):c.264G>A (p.Glu88=)	not provided [RCV003710898]	likely benign	2	215434709	215434709	Human		name
405186239	CV3040505	single nucleotide variant	NM_212482.4(FN1):c.156T>C (p.Cys52=)	not provided [RCV003706041]	likely benign	2	215434817	215434817	Human		name
597762858	CV3710128	single nucleotide variant	NM_212482.4(FN1):c.144C>T (p.Ser48=)	Glomerulopathy with fibronectin deposits 2 [RCV005018583]	uncertain significance	2	215435659	215435659	Human	1	name
597635303	CV3710134	single nucleotide variant	NM_212482.4(FN1):c.16G>A (p.Gly6Arg)	Glomerulopathy with fibronectin deposits 2 [RCV005024048]	uncertain significance	2	215435787	215435787	Human	1	name
597917822	CV3737758	single nucleotide variant	NM_133372.3(FNIP1):c.24G>A (p.Lys8=)	not provided [RCV005074357]	likely benign	5	131796898	131796898	Human		name
597927755	CV3749049	single nucleotide variant	NM_212482.4(FN1):c.138T>C (p.Ser46=)	not provided [RCV005075505]	likely benign	2	215435665	215435665	Human		name
597838794	CV3824842	single nucleotide variant	NM_212482.4(FN1):c.14C>G (p.Pro5Arg)	not provided [RCV005171706]	uncertain significance	2	215435789	215435789	Human		name
15156333	CV697306	single nucleotide variant	NM_212482.4(FN1):c.199C>A (p.Arg67=)	Glomerulopathy with fibronectin deposits 2 [RCV002489289]\|not provided [RCV000946676]	benign\|likely benign	2	215434774	215434774	Human	1	name
15106628	CV781160	single nucleotide variant	NM_212482.4(FN1):c.117C>G (p.Pro39=)	Glomerulopathy with fibronectin deposits 2 [RCV002479144]\|not provided [RCV000976666]	benign\|likely benign	2	215435686	215435686	Human	1	name
21068005	CV795154	single nucleotide variant	NM_212482.4(FN1):c.10G>A (p.Gly4Ser)	not provided [RCV000997658]	uncertain significance	2	215435793	215435793	Human		name
127232722	CV1090699	single nucleotide variant	NM_212482.4(FN1):c.456C>T (p.Asp152=)	not provided [RCV001421420]	likely benign	2	215431924	215431924	Human		name
127299086	CV1153985	single nucleotide variant	NM_212482.4(FN1):c.378C>T (p.Ile126=)	not provided [RCV001513544]	benign	2	215433361	215433361	Human		name
150528188	CV1301725	single nucleotide variant	NM_212482.4(FN1):c.91A>T (p.Arg31Trp)	not provided [RCV001755097]	uncertain significance	2	215435712	215435712	Human		name
151837107	CV1371493	single nucleotide variant	NM_212482.4(FN1):c.414A>G (p.Ala138=)	Glomerulopathy with fibronectin deposits 2 [RCV005016833]\|not provided [RCV001921100]	uncertain significance	2	215433325	215433325	Human	1	name
152060957	CV1540709	single nucleotide variant	NM_212482.4(FN1):c.471A>G (p.Pro157=)	not provided [RCV002110107]	likely benign	2	215431909	215431909	Human		name
152118332	CV1594894	single nucleotide variant	NM_212482.4(FN1):c.573T>C (p.Ala191=)	not provided [RCV002197702]	likely benign	2	215430827	215430827	Human		name
152116238	CV1610906	single nucleotide variant	NM_212482.4(FN1):c.375C>T (p.Cys125=)	not provided [RCV002135130]	likely benign	2	215433364	215433364	Human		name
156361543	CV1904905	single nucleotide variant	NM_212482.4(FN1):c.894T>C (p.Pro298=)	not provided [RCV002602533]	likely benign	2	215425236	215425236	Human		name
156437233	CV1937064	single nucleotide variant	NM_212482.4(FN1):c.411C>T (p.Ile137=)	not provided [RCV003106764]	likely benign	2	215433328	215433328	Human		name
156393624	CV1962521	single nucleotide variant	NM_212482.4(FN1):c.591C>G (p.Val197=)	not provided [RCV002584124]	likely benign	2	215430809	215430809	Human		name
156411421	CV1976294	single nucleotide variant	NM_212482.4(FN1):c.660C>T (p.Ser220=)	not provided [RCV002587487]	likely benign	2	215430740	215430740	Human		name
156302237	CV1998466	single nucleotide variant	NM_212482.4(FN1):c.840G>A (p.Ser280=)	not provided [RCV002671213]	likely benign	2	215428184	215428184	Human		name
156125475	CV2046705	single nucleotide variant	NM_212482.4(FN1):c.600G>A (p.Thr200=)	not provided [RCV002800399]	likely benign	2	215430800	215430800	Human		name
155904094	CV2084040	single nucleotide variant	NM_212482.4(FN1):c.762C>T (p.Asn254=)	not provided [RCV002858040]	likely benign	2	215428262	215428262	Human		name
155941702	CV2229268	single nucleotide variant	NM_133372.3(FNIP1):c.8C>G (p.Pro3Arg)	Inborn genetic diseases [RCV002752018]	uncertain significance	5	131796914	131796914	Human	1	name
156243079	CV2246314	single nucleotide variant	NM_002027.3(FNTA):c.13G>A (p.Glu5Lys)	not specified [RCV004107759]	uncertain significance	8	43056359	43056359	Human		name
156002225	CV2287978	single nucleotide variant	NM_002027.3(FNTA):c.16G>T (p.Gly6Trp)	not specified [RCV004147750]	uncertain significance	8	43056362	43056362	Human		name
156103851	CV2400242	single nucleotide variant	NM_002027.3(FNTA):c.19G>T (p.Val7Phe)	not specified [RCV004243034]	uncertain significance	8	43056365	43056365	Human		name
243053439	CV2410191	single nucleotide variant	NM_212482.4(FN1):c.74G>A (p.Gly25Glu)	not provided [RCV003144077]	conflicting interpretations of pathogenicity\|uncertain significance	2	215435729	215435729	Human		name
401727873	CV2678538	single nucleotide variant	NM_002028.4(FNTB):c.26A>G (p.Tyr9Cys)	not specified [RCV004292549]	uncertain significance	14	64986979	64986979	Human		name
402508087	CV2869636	single nucleotide variant	NM_133372.3(FNIP1):c.42C>T (p.Thr14=)	not provided [RCV003548898]	likely benign	5	131796880	131796880	Human		name
402499237	CV2871979	single nucleotide variant	NM_212482.4(FN1):c.46T>G (p.Cys16Gly)	not provided [RCV003545730]	likely benign	2	215435757	215435757	Human		name
405236857	CV2884779	single nucleotide variant	NM_212482.4(FN1):c.864T>C (p.Asp288=)	not provided [RCV003556569]	likely benign	2	215425266	215425266	Human		name
402489046	CV2995665	single nucleotide variant	NM_212482.4(FN1):c.45G>T (p.Gln15His)	not provided [RCV003687352]	uncertain significance	2	215435758	215435758	Human		name
402502675	CV3006988	variation	NM_212482.4(FN1):c.6781= (p.Val2261=)	not provided [RCV003688663]	uncertain significance	2	215370366	215370366	Human		name
402484512	CV3036845	single nucleotide variant	NM_212482.4(FN1):c.76G>A (p.Ala26Thr)	not provided [RCV003713167]	uncertain significance	2	215435727	215435727	Human		name
402474574	CV3042042	single nucleotide variant	NM_133372.3(FNIP1):c.75C>T (p.Asp25=)	not provided [RCV003710535]	likely benign	5	131796847	131796847	Human		name
405244989	CV3054855	single nucleotide variant	NM_212482.4(FN1):c.591C>T (p.Val197=)	not provided [RCV003720155]	likely benign	2	215430809	215430809	Human		name
405220005	CV3059791	single nucleotide variant	NM_212482.4(FN1):c.888G>A (p.Pro296=)	not provided [RCV003733163]	likely benign	2	215425242	215425242	Human		name
405241963	CV3078552	single nucleotide variant	NM_212482.4(FN1):c.855C>T (p.Pro285=)	not provided [RCV003737473]	likely benign	2	215425275	215425275	Human		name
405085218	CV3122006	single nucleotide variant	NM_212482.4(FN1):c.858C>T (p.Phe286=)	not provided [RCV003810761]	benign	2	215425272	215425272	Human		name
405142581	CV3126002	single nucleotide variant	NM_212482.4(FN1):c.843C>T (p.Ser281=)	Glomerulopathy with fibronectin deposits 2 [RCV005014989]\|not provided [RCV003816918]	uncertain significance	2	215428181	215428181	Human	1	name
405009788	CV3127967	single nucleotide variant	NM_212482.4(FN1):c.696C>T (p.Asn232=)	not provided [RCV003828847]	likely benign	2	215428328	215428328	Human		name
405238305	CV3169608	single nucleotide variant	NM_212482.4(FN1):c.95A>C (p.Gln32Pro)	Inborn genetic diseases [RCV005335957]\|not provided [RCV003866696]	uncertain significance	2	215435708	215435708	Human	1	name
402504284	CV3181452	single nucleotide variant	NM_212482.4(FN1):c.789C>T (p.Asn263=)	not provided [RCV003878286]	likely benign	2	215428235	215428235	Human		name
404984535	CV3183659	single nucleotide variant	NM_212482.4(FN1):c.600G>T (p.Thr200=)	not provided [RCV003880936]	likely benign	2	215430800	215430800	Human		name
405745958	CV3253760	single nucleotide variant	NM_002027.3(FNTA):c.22G>A (p.Gly8Arg)	not specified [RCV004392024]	uncertain significance	8	43056368	43056368	Human		name
597635310	CV3710131	single nucleotide variant	NM_212482.4(FN1):c.87C>A (p.Ser29Arg)	Glomerulopathy with fibronectin deposits 2 [RCV005024047]\|not provided [RCV005112757]	likely benign\|uncertain significance	2	215435716	215435716	Human	1	name
597762870	CV3710132	single nucleotide variant	NM_212482.4(FN1):c.61G>A (p.Val21Met)	Glomerulopathy with fibronectin deposits 2 [RCV005018585]\|not provided [RCV005112758]	uncertain significance	2	215435742	215435742	Human	1	name
597762877	CV3710133	single nucleotide variant	NM_212482.4(FN1):c.59C>A (p.Ala20Glu)	Glomerulopathy with fibronectin deposits 2 [RCV005018586]\|not provided [RCV005063244]	uncertain significance	2	215435744	215435744	Human	1	name
597880292	CV3744804	single nucleotide variant	NM_212482.4(FN1):c.693C>T (p.Cys231=)	not provided [RCV005069829]	likely benign	2	215428331	215428331	Human		name
597973745	CV3820680	single nucleotide variant	NM_212482.4(FN1):c.309G>C (p.Gly103=)	not provided [RCV005168197]	benign	2	215433430	215433430	Human		name
597942253	CV3847213	single nucleotide variant	NM_212482.4(FN1):c.849T>C (p.Ser283=)	not provided [RCV005188133]	likely benign	2	215425281	215425281	Human		name
15174313	CV708017	single nucleotide variant	NM_212482.4(FN1):c.40G>C (p.Val14Leu)	not provided [RCV000972693]	benign\|likely benign	2	215435763	215435763	Human		name
15109536	CV719599	single nucleotide variant	NM_212482.4(FN1):c.591C>A (p.Val197=)	not provided [RCV000893884]	benign	2	215430809	215430809	Human		name
15184379	CV719602	single nucleotide variant	NM_212482.4(FN1):c.56C>T (p.Thr19Ile)	not provided [RCV000886433]	benign\|likely benign	2	215435747	215435747	Human		name
15172991	CV724476	single nucleotide variant	NM_015308.5(FNBP4):c.33T>C (p.Arg11=)	not provided [RCV000883951]	benign	11	47767256	47767256	Human		name
15119302	CV733150	single nucleotide variant	NM_212482.4(FN1):c.939T>C (p.Gly313=)	not provided [RCV000895701]	likely benign	2	215425191	215425191	Human		name
15166095	CV738022	single nucleotide variant	NM_015308.5(FNBP4):c.78G>T (p.Thr26=)	not provided [RCV000904367]	benign	11	47767211	47767211	Human		name
15098422	CV747281	single nucleotide variant	NM_212482.4(FN1):c.861C>T (p.Thr287=)	not provided [RCV000914244]	likely benign	2	215425269	215425269	Human		name
21071091	CV790195	single nucleotide variant	NM_212482.4(FN1):c.44A>T (p.Gln15Leu)	Glomerulopathy with fibronectin deposits 2 [RCV001702076]\|Spondyloepimetaphyseal dysplasia, Strudwick type [RCV000987029]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702874]\|not provided [RCV001521856]\|not specified [RCV001529025]	benign	2	215435759	215435759	Human	27	name
21071091	CV790195	single nucleotide variant	NM_212482.4(FN1):c.44A>T (p.Gln15Leu)	Glomerulopathy with fibronectin deposits 2 [RCV001702076]\|Spondyloepimetaphyseal dysplasia, Strudwick type [RCV000987029]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702874]\|not provided [RCV001521856]\|not specified [RCV001529025]	benign	2	215435759	215435760	Human	27	name
126768020	CV1003660	single nucleotide variant	NM_212482.4(FN1):c.125C>T (p.Pro42Leu)	not provided [RCV001321118]	uncertain significance	2	215435678	215435678	Human		name
127260227	CV1069021	single nucleotide variant	NM_212482.4(FN1):c.1413A>C (p.Thr471=)	Glomerulopathy with fibronectin deposits 2 [RCV002476739]\|not provided [RCV001402142]	likely benign	2	215422224	215422224	Human	1	name
127297875	CV1112235	single nucleotide variant	NM_212482.4(FN1):c.1764C>T (p.Tyr588=)	not provided [RCV001453159]	likely benign	2	215419297	215419297	Human		name
127318880	CV1153981	single nucleotide variant	NM_212482.4(FN1):c.2442T>A (p.Pro814=)	Glomerulopathy with fibronectin deposits 2 [RCV001702113]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702114]\|not provided [RCV001521855]\|not specified [RCV001529219]	benign	2	215408184	215408184	Human	2	name
150534072	CV1300383	deletion	NM_212482.4(FN1):c.582del (p.Tyr195fs)	not provided [RCV001758511]	uncertain significance	2	215430818	215430818	Human		name
151728521	CV1486734	single nucleotide variant	NM_212482.4(FN1):c.1674C>T (p.Val558=)	not provided [RCV001892000]	uncertain significance	2	215420674	215420674	Human		name
151785956	CV1494021	single nucleotide variant	NM_212482.4(FN1):c.2244G>A (p.Ser748=)	not provided [RCV001951543]	likely benign	2	215409618	215409618	Human		name
152118125	CV1534870	single nucleotide variant	NM_212482.4(FN1):c.1521A>G (p.Thr507=)	not provided [RCV002153908]	likely benign	2	215422116	215422116	Human		name
152097582	CV1542291	single nucleotide variant	NM_212482.4(FN1):c.2145G>A (p.Thr715=)	not provided [RCV002195125]	likely benign	2	215409717	215409717	Human		name
152159936	CV1544501	single nucleotide variant	NM_212482.4(FN1):c.2187C>T (p.Thr729=)	not provided [RCV002123006]	benign	2	215409675	215409675	Human		name
152072639	CV1551675	single nucleotide variant	NM_212482.4(FN1):c.1614G>A (p.Gly538=)	not provided [RCV002075309]	likely benign	2	215420734	215420734	Human		name
152125185	CV1554022	single nucleotide variant	NM_212482.4(FN1):c.2061C>T (p.Tyr687=)	not provided [RCV002098720]	likely benign	2	215409995	215409995	Human		name
152145103	CV1576651	single nucleotide variant	NM_212482.4(FN1):c.1371G>A (p.Lys457=)	not provided [RCV002101341]	likely benign	2	215423372	215423372	Human		name
152128162	CV1583720	single nucleotide variant	NM_212482.4(FN1):c.1884C>A (p.Ile628=)	not provided [RCV002198965]	likely benign	2	215414894	215414894	Human		name
152092839	CV1593219	single nucleotide variant	NM_212482.4(FN1):c.1014C>T (p.Asn338=)	not provided [RCV002094426]	likely benign	2	215425116	215425116	Human		name
152037231	CV1605555	single nucleotide variant	NM_212482.4(FN1):c.2007A>G (p.Lys669=)	not provided [RCV002087421]	likely benign	2	215410049	215410049	Human		name
152156113	CV1615710	single nucleotide variant	NM_212482.4(FN1):c.2091C>T (p.Phe697=)	not provided [RCV002158872]	benign	2	215409965	215409965	Human		name
152118373	CV1620183	single nucleotide variant	NM_212482.4(FN1):c.1185C>T (p.Asp395=)	not provided [RCV002216446]	likely benign	2	215424177	215424177	Human		name
152141342	CV1625805	single nucleotide variant	NM_212482.4(FN1):c.1299T>C (p.Asp433=)	not provided [RCV002138217]	likely benign	2	215423444	215423444	Human		name
152089002	CV1639002	single nucleotide variant	NM_212482.4(FN1):c.2031C>T (p.Tyr677=)	not provided [RCV002150342]	likely benign	2	215410025	215410025	Human		name
152032873	CV1643200	single nucleotide variant	NM_212482.4(FN1):c.2967G>C (p.Leu989=)	Glomerulopathy with fibronectin deposits 2 [RCV002498214]\|not provided [RCV002205063]	likely benign	2	215406257	215406257	Human	1	name
152035133	CV1670096	single nucleotide variant	NM_212482.4(FN1):c.2112A>G (p.Thr704=)	not provided [RCV002223630]	conflicting interpretations of pathogenicity\|uncertain significance	2	215409944	215409944	Human		name
152985502	CV1675360	single nucleotide variant	NM_212482.4(FN1):c.261C>G (p.Cys87Trp)	Spondylometaphyseal dysplasia - Sutcliffe type [RCV002240143]\|not provided [RCV003698884]	pathogenic	2	215434712	215434712	Human	1	name
156352728	CV1893380	single nucleotide variant	NM_212482.4(FN1):c.1170G>A (p.Ser390=)	not provided [RCV003091106]	likely benign	2	215424192	215424192	Human		name
156360124	CV1910850	single nucleotide variant	NM_212482.4(FN1):c.2238C>T (p.Thr746=)	not provided [RCV002632618]	likely benign	2	215409624	215409624	Human		name
156205369	CV1913137	single nucleotide variant	NM_133372.3(FNIP1):c.294C>T (p.Ser98=)	not provided [RCV002595863]	likely benign	5	131730964	131730964	Human		name
156434638	CV1940143	single nucleotide variant	NM_212482.4(FN1):c.2358C>T (p.Tyr786=)	not provided [RCV003104557]	likely benign	2	215408368	215408368	Human		name
156244353	CV1956872	single nucleotide variant	NM_212482.4(FN1):c.2307A>G (p.Pro769=)	not provided [RCV002576331]	benign	2	215408419	215408419	Human		name
156251254	CV1984787	single nucleotide variant	NM_133372.3(FNIP1):c.252T>C (p.Phe84=)	not provided [RCV002645904]	likely benign	5	131731006	131731006	Human		name
156011124	CV1991912	single nucleotide variant	NM_212482.4(FN1):c.2715T>C (p.Asp905=)	not provided [RCV002618910]	likely benign\|uncertain significance	2	215406509	215406509	Human		name
156111386	CV1997052	single nucleotide variant	NM_212482.4(FN1):c.2760C>T (p.Asp920=)	not provided [RCV002662503]	likely benign	2	215406464	215406464	Human		name
156121416	CV1998243	single nucleotide variant	NM_212482.4(FN1):c.1338T>C (p.Cys446=)	not provided [RCV002662869]	likely benign	2	215423405	215423405	Human		name
156275156	CV2004897	single nucleotide variant	NM_212482.4(FN1):c.2730C>A (p.Pro910=)	not provided [RCV002646662]	likely benign	2	215406494	215406494	Human		name
156092724	CV2014064	single nucleotide variant	NM_212482.4(FN1):c.2697T>C (p.Thr899=)	not provided [RCV002695001]	likely benign	2	215407143	215407143	Human		name
155925046	CV2045014	single nucleotide variant	NM_212482.4(FN1):c.1584C>T (p.Asn528=)	not provided [RCV002750891]	likely benign	2	215420764	215420764	Human		name
156322095	CV2067658	single nucleotide variant	NM_212482.4(FN1):c.143G>A (p.Ser48Asn)	not provided [RCV002834771]	uncertain significance	2	215435660	215435660	Human		name
156325075	CV2068481	single nucleotide variant	NM_212482.4(FN1):c.2844C>T (p.Gly948=)	not provided [RCV002834965]	uncertain significance	2	215406380	215406380	Human		name
156151158	CV2070297	single nucleotide variant	NM_212482.4(FN1):c.191A>G (p.Gln64Arg)	Glomerulopathy with fibronectin deposits 2 [RCV005019410]\|not provided [RCV002850873]	uncertain significance	2	215434782	215434782	Human	1	name
155946647	CV2077099	single nucleotide variant	NM_133372.3(FNIP1):c.216A>G (p.Val72=)	not provided [RCV002880258]	likely benign	5	131744567	131744567	Human		name
156145890	CV2078679	single nucleotide variant	NM_133372.3(FNIP1):c.282A>G (p.Gly94=)	not provided [RCV002872150]	likely benign	5	131730976	131730976	Human		name
156148204	CV2078782	single nucleotide variant	NM_212482.4(FN1):c.2106C>T (p.Thr702=)	not provided [RCV002872228]	likely benign	2	215409950	215409950	Human		name
156108949	CV2085690	single nucleotide variant	NM_212482.4(FN1):c.1653C>T (p.Gly551=)	not provided [RCV002848371]	uncertain significance	2	215420695	215420695	Human		name
155960432	CV2088965	single nucleotide variant	NM_212482.4(FN1):c.1140G>A (p.Gln380=)	not provided [RCV002880990]	likely benign	2	215424222	215424222	Human		name
156032436	CV2132704	single nucleotide variant	NM_212482.4(FN1):c.2850C>T (p.His950=)	not provided [RCV002999199]	likely benign	2	215406374	215406374	Human		name
156278648	CV2164559	single nucleotide variant	NM_212482.4(FN1):c.176A>G (p.Tyr59Cys)	not provided [RCV003027240]	uncertain significance	2	215434797	215434797	Human		name
156225060	CV2176363	single nucleotide variant	NM_212482.4(FN1):c.1680A>G (p.Gln560=)	not provided [RCV003059095]	likely benign	2	215419381	215419381	Human		name
156175499	CV2181423	single nucleotide variant	NM_212482.4(FN1):c.1233A>T (p.Arg411=)	not provided [RCV003057356]	likely benign	2	215423510	215423510	Human		name
156044143	CV2215905	single nucleotide variant	NM_212482.4(FN1):c.200G>A (p.Arg67Gln)	Inborn genetic diseases [RCV002692459]	uncertain significance	2	215434773	215434773	Human	1	name
156264035	CV2329415	single nucleotide variant	NM_022158.4(FN3K):c.38C>T (p.Thr13Ile)	not specified [RCV004187423]	uncertain significance	17	82735674	82735674	Human		name
156103317	CV2386896	single nucleotide variant	NM_002028.4(FNTB):c.29A>G (p.Tyr10Cys)	not specified [RCV004233529]	uncertain significance	14	64986982	64986982	Human		name
329396378	CV2459604	single nucleotide variant	NM_002028.4(FNTB):c.85G>A (p.Glu29Lys)	not specified [RCV004277050]	uncertain significance	14	64987038	64987038	Human		name
329399904	CV2467678	single nucleotide variant	NM_212482.4(FN1):c.278C>A (p.Ala93Asp)	Glomerulopathy with fibronectin deposits 2 [RCV004818298]\|Inborn genetic diseases [RCV003221141]	uncertain significance	2	215433461	215433461	Human	2	name
401764781	CV2705345	single nucleotide variant	NM_002028.4(FNTB):c.64C>T (p.Pro22Ser)	not specified [RCV004312023]	uncertain significance	14	64987017	64987017	Human		name
401903265	CV2810511	single nucleotide variant	NM_002028.4(FNTB):c.672C>T (p.Gly224=)	not provided [RCV003411039]	likely benign	14	65032676	65032676	Human		name
401903268	CV2810512	single nucleotide variant	NM_002028.4(FNTB):c.915G>A (p.Ala305=)	not provided [RCV003411040]	likely benign	14	65044403	65044403	Human		name
401902793	CV2810513	single nucleotide variant	NM_002028.4(FNTB):c.990C>T (p.Phe330=)	not provided [RCV003400590]	benign	14	65053272	65053272	Human		name
405041090	CV2862695	single nucleotide variant	NM_212482.4(FN1):c.2868C>T (p.Ile956=)	not provided [RCV003579116]	likely benign	2	215406356	215406356	Human		name
405218732	CV2869894	single nucleotide variant	NM_212482.4(FN1):c.218C>T (p.Ala73Val)	not provided [RCV003553563]	uncertain significance	2	215434755	215434755	Human		name
405074743	CV2940670	single nucleotide variant	NM_133372.3(FNIP1):c.237T>C (p.Ala79=)	not provided [RCV003659633]	likely benign	5	131731021	131731021	Human		name
405088914	CV2943476	single nucleotide variant	NM_212482.4(FN1):c.1917C>T (p.Ser639=)	not provided [RCV003665149]	likely benign	2	215414861	215414861	Human		name
405078430	CV2945383	single nucleotide variant	NM_212482.4(FN1):c.136A>G (p.Ser46Gly)	not provided [RCV003664424]	uncertain significance	2	215435667	215435667	Human		name
405116408	CV2961646	single nucleotide variant	NM_212482.4(FN1):c.1794T>C (p.His598=)	not provided [RCV003670996]	likely benign	2	215419267	215419267	Human		name
405138954	CV2963343	single nucleotide variant	NM_212482.4(FN1):c.2658T>C (p.Asn886=)	not provided [RCV003668960]	likely benign	2	215407182	215407182	Human		name
405219915	CV2969553	single nucleotide variant	NM_212482.4(FN1):c.1404A>G (p.Glu468=)	not provided [RCV003680524]	likely benign	2	215422233	215422233	Human		name
405197271	CV2972788	single nucleotide variant	NM_212482.4(FN1):c.1206A>G (p.Thr402=)	not provided [RCV003677800]	likely benign	2	215424156	215424156	Human		name
402489973	CV2984460	single nucleotide variant	NM_212482.4(FN1):c.2262T>C (p.Tyr754=)	not provided [RCV003713619]	likely benign	2	215409600	215409600	Human		name
405115767	CV2996469	single nucleotide variant	NM_212482.4(FN1):c.176A>T (p.Tyr59Phe)	not provided [RCV003723340]	uncertain significance	2	215434797	215434797	Human		name
405117431	CV3020352	single nucleotide variant	NM_212482.4(FN1):c.1788G>A (p.Glu596=)	not provided [RCV003700387]	likely benign	2	215419273	215419273	Human		name
405185204	CV3040358	single nucleotide variant	NM_212482.4(FN1):c.2814T>A (p.Arg938=)	not provided [RCV003705950]	likely benign	2	215406410	215406410	Human		name
405224660	CV3058191	single nucleotide variant	NM_212482.4(FN1):c.1536G>A (p.Ser512=)	not provided [RCV003733838]	likely benign	2	215422101	215422101	Human		name
405194678	CV3062872	single nucleotide variant	NM_212482.4(FN1):c.2899C>T (p.Leu967=)	not provided [RCV003730062]	likely benign	2	215406325	215406325	Human		name
405205770	CV3068110	single nucleotide variant	NM_212482.4(FN1):c.1941T>G (p.Pro647=)	not provided [RCV003731245]	uncertain significance	2	215414837	215414837	Human		name
404989331	CV3131896	single nucleotide variant	NM_212482.4(FN1):c.2628T>C (p.Tyr876=)	not provided [RCV003827024]	likely benign	2	215407212	215407212	Human		name
405091435	CV3134474	single nucleotide variant	NM_212482.4(FN1):c.1548T>C (p.Asp516=)	not provided [RCV003834820]	likely benign	2	215420800	215420800	Human		name
405158985	CV3152694	single nucleotide variant	NM_212482.4(FN1):c.2457G>A (p.Val819=)	not provided [RCV003840621]	likely benign	2	215408169	215408169	Human		name
405140784	CV3155266	single nucleotide variant	NM_133372.3(FNIP1):c.159A>G (p.Arg53=)	not provided [RCV003855504]	likely benign	5	131744624	131744624	Human		name
405246715	CV3158567	single nucleotide variant	NM_212482.4(FN1):c.2571C>T (p.Asn857=)	not provided [RCV003868909]	likely benign	2	215407269	215407269	Human		name
405215144	CV3160666	single nucleotide variant	NM_212482.4(FN1):c.242G>A (p.Gly81Glu)	not provided [RCV003862728]	uncertain significance	2	215434731	215434731	Human		name
405156188	CV3163471	single nucleotide variant	NM_212482.4(FN1):c.253T>G (p.Phe85Val)	not provided [RCV003856717]	uncertain significance	2	215434720	215434720	Human		name
402484991	CV3171292	single nucleotide variant	NM_212482.4(FN1):c.2835C>T (p.Asn945=)	not provided [RCV003876319]	benign	2	215406389	215406389	Human		name
402469855	CV3174856	single nucleotide variant	NM_212482.4(FN1):c.2430G>A (p.Ala810=)	not provided [RCV003873967]	likely benign	2	215408196	215408196	Human		name
405230035	CV3176710	single nucleotide variant	NM_212482.4(FN1):c.1245C>T (p.Ser415=)	not provided [RCV003865084]	likely benign	2	215423498	215423498	Human		name
402465264	CV3177155	single nucleotide variant	NM_212482.4(FN1):c.1713A>G (p.Gln571=)	not provided [RCV003872786]	likely benign	2	215419348	215419348	Human		name
405227783	CV3180258	single nucleotide variant	NM_212482.4(FN1):c.1206A>C (p.Thr402=)	not provided [RCV003864678]	likely benign	2	215424156	215424156	Human		name
405745994	CV3253764	single nucleotide variant	NM_002027.3(FNTA):c.41G>A (p.Gly14Asp)	not specified [RCV004392028]	uncertain significance	8	43056387	43056387	Human		name
405746064	CV3253774	single nucleotide variant	NM_002028.4(FNTB):c.97G>C (p.Glu33Gln)	not specified [RCV004392038]	uncertain significance	14	64987050	64987050	Human		name
407510137	CV3432477	single nucleotide variant	NM_022158.4(FN3K):c.49T>G (p.Phe17Val)	not specified [RCV004625997]	uncertain significance	17	82735685	82735685	Human		name
597725129	CV3672895	single nucleotide variant	NM_020840.3(FNIP2):c.25C>G (p.Leu9Val)	not specified [RCV004919169]	uncertain significance	4	158769237	158769237	Human		name
597725228	CV3672911	single nucleotide variant	NM_002028.4(FNTB):c.98A>G (p.Glu33Gly)	not specified [RCV004919183]	uncertain significance	14	64987051	64987051	Human		name
597762683	CV3710084	single nucleotide variant	NM_212482.4(FN1):c.2427A>G (p.Thr809=)	Glomerulopathy with fibronectin deposits 2 [RCV005018549]	uncertain significance	2	215408299	215408299	Human	1	name
597635383	CV3710085	single nucleotide variant	NM_212482.4(FN1):c.2421A>G (p.Gln807=)	Glomerulopathy with fibronectin deposits 2 [RCV005024035]	uncertain significance	2	215408305	215408305	Human	1	name
597635321	CV3710124	single nucleotide variant	NM_212482.4(FN1):c.286A>T (p.Thr96Ser)	Glomerulopathy with fibronectin deposits 2 [RCV005024045]	uncertain significance	2	215433453	215433453	Human	1	name
597762841	CV3710125	single nucleotide variant	NM_212482.4(FN1):c.239G>C (p.Gly80Ala)	Glomerulopathy with fibronectin deposits 2 [RCV005018580]	uncertain significance	2	215434734	215434734	Human	1	name
597762853	CV3710127	single nucleotide variant	NM_212482.4(FN1):c.163A>G (p.Asn55Asp)	Glomerulopathy with fibronectin deposits 2 [RCV005018582]	uncertain significance	2	215434810	215434810	Human	1	name
597762865	CV3710129	single nucleotide variant	NM_212482.4(FN1):c.131C>T (p.Ala44Val)	Glomerulopathy with fibronectin deposits 2 [RCV005018584]	uncertain significance	2	215435672	215435672	Human	1	name
597635316	CV3710130	single nucleotide variant	NM_212482.4(FN1):c.104A>G (p.Gln35Arg)	Glomerulopathy with fibronectin deposits 2 [RCV005024046]	uncertain significance	2	215435699	215435699	Human	1	name
597848721	CV3736860	single nucleotide variant	NM_212482.4(FN1):c.2133G>A (p.Val711=)	not provided [RCV005066019]	likely benign	2	215409729	215409729	Human		name
597919830	CV3738006	single nucleotide variant	NM_212482.4(FN1):c.2895C>T (p.Thr965=)	not provided [RCV005074605]	likely benign	2	215406329	215406329	Human		name
597835580	CV3739707	single nucleotide variant	NM_212482.4(FN1):c.2613A>G (p.Gln871=)	not provided [RCV005063927]	likely benign	2	215407227	215407227	Human		name
597904973	CV3742038	single nucleotide variant	NM_212482.4(FN1):c.2787G>A (p.Pro929=)	not provided [RCV005072822]	benign	2	215406437	215406437	Human		name
597830955	CV3743713	single nucleotide variant	NM_212482.4(FN1):c.1836C>T (p.Val612=)	not provided [RCV005062530]	likely benign	2	215414942	215414942	Human		name
597876873	CV3747912	single nucleotide variant	NM_212482.4(FN1):c.2145G>T (p.Thr715=)	not provided [RCV005069404]	likely benign	2	215409717	215409717	Human		name
597835960	CV3761058	single nucleotide variant	NM_212482.4(FN1):c.2274G>A (p.Glu758=)	not provided [RCV005085609]	likely benign	2	215409588	215409588	Human		name
597895774	CV3773487	single nucleotide variant	NM_212482.4(FN1):c.2163T>A (p.Leu721=)	not provided [RCV005111394]	likely benign	2	215409699	215409699	Human		name
597888433	CV3787742	single nucleotide variant	NM_212482.4(FN1):c.229A>C (p.Thr77Pro)	not provided [RCV005125309]	uncertain significance	2	215434744	215434744	Human		name
597974425	CV3802170	single nucleotide variant	NM_133372.3(FNIP1):c.162G>A (p.Gly54=)	not provided [RCV005143946]	likely benign	5	131744621	131744621	Human		name
597854690	CV3825091	single nucleotide variant	NM_133372.3(FNIP1):c.132G>A (p.Leu44=)	not provided [RCV005173939]	likely benign	5	131744651	131744651	Human		name
597831375	CV3830761	single nucleotide variant	NM_212482.4(FN1):c.284A>T (p.Glu95Val)	not provided [RCV005170159]	uncertain significance	2	215433455	215433455	Human		name
597940069	CV3836567	single nucleotide variant	NM_212482.4(FN1):c.2685A>G (p.Gln895=)	not provided [RCV005187588]	likely benign	2	215407155	215407155	Human		name
597943440	CV3847676	single nucleotide variant	NM_212482.4(FN1):c.1116C>T (p.Tyr372=)	not provided [RCV005188404]	likely benign	2	215424246	215424246	Human		name
597937006	CV3862464	single nucleotide variant	NM_212482.4(FN1):c.1881C>G (p.Pro627=)	not provided [RCV005207736]	likely benign	2	215414897	215414897	Human		name
598215056	CV3973497	single nucleotide variant	NM_212482.4(FN1):c.140A>G (p.Gln47Arg)	Inborn genetic diseases [RCV005339627]	uncertain significance	2	215435663	215435663	Human	1	name
598215090	CV3973504	single nucleotide variant	NM_022158.4(FN3K):c.31A>T (p.Thr11Ser)	not specified [RCV005339634]	uncertain significance	17	82735667	82735667	Human		name
598215315	CV3973549	single nucleotide variant	NM_032532.3(FNDC1):c.16G>C (p.Gly6Arg)	not specified [RCV005339677]	uncertain significance	6	159169612	159169612	Human		name
598215461	CV3973580	single nucleotide variant	NM_022763.4(FNDC3B):c.7G>A (p.Val3Ile)	not specified [RCV005339706]	uncertain significance	3	172112486	172112486	Human		name
598215495	CV3973587	single nucleotide variant	NM_022823.3(FNDC4):c.23C>T (p.Ser8Phe)	not specified [RCV005339712]	uncertain significance	2	27494657	27494657	Human		name
598215631	CV3973615	single nucleotide variant	NM_133372.3(FNIP1):c.11C>T (p.Thr4Met)	Inborn genetic diseases [RCV005339737]	uncertain significance	5	131796911	131796911	Human	1	name
617153576	CV4020855	single nucleotide variant	NM_002028.4(FNTB):c.771C>T (p.Ala257=)	not provided [RCV005428608]	likely benign	14	65040868	65040868	Human		name
617153578	CV4020906	single nucleotide variant	NM_002028.4(FNTB):c.585C>T (p.Val195=)	not provided [RCV005428659]	likely benign	14	65027761	65027761	Human		name
617153558	CV4021935	single nucleotide variant	NM_002028.4(FNTB):c.474T>C (p.Asn158=)	not provided [RCV005426896]	likely benign	14	65027552	65027552	Human		name
13442864	CV411549	single nucleotide variant	NM_212482.4(FN1):c.260G>T (p.Cys87Phe)	Spondylometaphyseal dysplasia - Sutcliffe type [RCV000566441]\|Spondylometaphyseal dysplasia [RCV000509586]	pathogenic\|likely pathogenic	2	215434713	215434713	Human	3	name
15156323	CV697303	single nucleotide variant	NM_212482.4(FN1):c.1530C>T (p.Ala510=)	not provided [RCV000946674]	benign\|likely benign	2	215422107	215422107	Human		name
15156328	CV697304	single nucleotide variant	NM_212482.4(FN1):c.1425G>C (p.Gly475=)	Glomerulopathy with fibronectin deposits 2 [RCV002502904]\|not provided [RCV000946675]	benign\|likely benign	2	215422212	215422212	Human	1	name
15165581	CV697305	single nucleotide variant	NM_212482.4(FN1):c.1110G>A (p.Thr370=)	Glomerulopathy with fibronectin deposits 2 [RCV002489296]\|not provided [RCV000948624]	benign\|likely benign	2	215424252	215424252	Human	1	name
15158623	CV700595	single nucleotide variant	NM_002027.3(FNTA):c.927C>A (p.Pro309=)	not provided [RCV000947108]	benign	8	43084791	43084791	Human		name
15174299	CV708012	single nucleotide variant	NM_212482.4(FN1):c.2592C>T (p.Ser864=)	not provided [RCV000972691]	benign\|likely benign	2	215407248	215407248	Human		name
15174308	CV708014	single nucleotide variant	NM_212482.4(FN1):c.1101T>C (p.Asn367=)	Glomerulopathy with fibronectin deposits 2 [RCV002505478]\|not provided [RCV000972692]	benign\|likely benign	2	215424261	215424261	Human	1	name
15166432	CV708016	single nucleotide variant	NM_212482.4(FN1):c.1023C>T (p.Ser341=)	Glomerulopathy with fibronectin deposits 2 [RCV002505472]\|not provided [RCV000971178]	benign\|likely benign	2	215425107	215425107	Human	1	name
15193985	CV719598	single nucleotide variant	NM_212482.4(FN1):c.1200C>T (p.Phe400=)	not provided [RCV000889095]	likely benign	2	215424162	215424162	Human		name
15163208	CV733149	single nucleotide variant	NM_212482.4(FN1):c.2829C>T (p.Pro943=)	Glomerulopathy with fibronectin deposits 2 [RCV002502678]\|not provided [RCV000903721]	benign\|likely benign	2	215406395	215406395	Human	1	name
15161704	CV733152	single nucleotide variant	NM_212482.4(FN1):c.121T>G (p.Ser41Ala)	not provided [RCV000903401]	benign\|likely benign	2	215435682	215435682	Human		name
15115524	CV747273	single nucleotide variant	NM_212482.4(FN1):c.2772C>T (p.Thr924=)	not provided [RCV000917469]	likely benign	2	215406452	215406452	Human		name
15203407	CV747274	single nucleotide variant	NM_212482.4(FN1):c.2538G>A (p.Ser846=)	Glomerulopathy with fibronectin deposits 2 [RCV002479060]\|not provided [RCV000913958]	likely benign	2	215407302	215407302	Human	1	name
15195500	CV747276	single nucleotide variant	NM_212482.4(FN1):c.2130C>T (p.Thr710=)	Glomerulopathy with fibronectin deposits 2 [RCV002505338]\|not provided [RCV000911434]	benign\|likely benign	2	215409732	215409732	Human	1	name
15106223	CV747277	single nucleotide variant	NM_212482.4(FN1):c.1923C>T (p.Tyr641=)	not provided [RCV000915704]	likely benign	2	215414855	215414855	Human		name
15199911	CV747278	single nucleotide variant	NM_212482.4(FN1):c.1449G>A (p.Gln483=)	Glomerulopathy with fibronectin deposits 2 [RCV002505344]\|not provided [RCV000912690]	likely benign	2	215422188	215422188	Human	1	name
15139818	CV747280	single nucleotide variant	NM_212482.4(FN1):c.1143C>T (p.Asp381=)	Glomerulopathy with fibronectin deposits 2 [RCV002502798]\|not provided [RCV000921575]	benign\|likely benign	2	215424219	215424219	Human	1	name
15098799	CV762889	single nucleotide variant	NM_212482.4(FN1):c.1638C>T (p.Phe546=)	Glomerulopathy with fibronectin deposits 2 [RCV002488015]\|not provided [RCV000936358]	likely benign	2	215420710	215420710	Human	1	name
15102110	CV762891	single nucleotide variant	NM_212482.4(FN1):c.1398C>T (p.His466=)	not provided [RCV000936928]	likely benign	2	215422239	215422239	Human		name
15183410	CV762892	single nucleotide variant	NM_212482.4(FN1):c.1062C>T (p.Asn354=)	not provided [RCV000930583]	likely benign	2	215424300	215424300	Human		name
15118631	CV762893	single nucleotide variant	NM_212482.4(FN1):c.1053C>T (p.Tyr351=)	Glomerulopathy with fibronectin deposits 2 [RCV002502878]\|not provided [RCV000940045]	likely benign	2	215424309	215424309	Human	1	name
15139751	CV781159	single nucleotide variant	NM_212482.4(FN1):c.1671C>T (p.Pro557=)	not provided [RCV000982692]	benign	2	215420677	215420677	Human		name
8636083	CV91306	single nucleotide variant	NM_017559.2(FNDC8):c.285G>A (p.Leu95=)	Malignant melanoma [RCV000071404]	not provided	17	35127117	35127117	Human		name
126747422	CV988359	single nucleotide variant	NM_212482.4(FN1):c.141A>C (p.Gln47His)	Glomerulopathy with fibronectin deposits 2 [RCV002493561]\|not provided [RCV001296732]	likely benign\|uncertain significance	2	215435662	215435662	Human	1	name
126766851	CV1003658	single nucleotide variant	NM_212482.4(FN1):c.869G>A (p.Arg290His)	Glomerulopathy with fibronectin deposits 2 [RCV002499621]\|Inborn genetic diseases [RCV004035012]\|not provided [RCV001320616]	likely benign\|uncertain significance	2	215425261	215425261	Human	2	name
126751205	CV1003659	single nucleotide variant	NM_212482.4(FN1):c.514A>G (p.Asn172Asp)	Inborn genetic diseases [RCV002546203]\|not provided [RCV001326869]	uncertain significance	2	215431866	215431866	Human	1	name
126923533	CV1041059	single nucleotide variant	NM_212482.4(FN1):c.412G>A (p.Ala138Thr)	Inborn genetic diseases [RCV004980385]\|not provided [RCV001365953]	likely benign\|uncertain significance	2	215433327	215433327	Human	1	name
126918120	CV1041060	single nucleotide variant	NM_212482.4(FN1):c.320G>C (p.Arg107Pro)	Inborn genetic diseases [RCV002548662]\|not provided [RCV001372471]	uncertain significance	2	215433419	215433419	Human	1	name
127249836	CV1055193	single nucleotide variant	NM_212482.4(FN1):c.674G>T (p.Cys225Phe)	not provided [RCV001378235]	pathogenic\|likely pathogenic	2	215430726	215430726	Human		name
127252899	CV1090694	single nucleotide variant	NM_212482.4(FN1):c.5160A>C (p.Val1720=)	not provided [RCV001425905]	likely benign	2	215382216	215382216	Human		name
127247854	CV1090695	single nucleotide variant	NM_212482.4(FN1):c.4926C>T (p.Thr1642=)	not provided [RCV001435702]	likely benign	2	215383452	215383452	Human		name
127237225	CV1090696	single nucleotide variant	NM_212482.4(FN1):c.4536C>A (p.Gly1512=)	not provided [RCV001433498]	likely benign	2	215386765	215386765	Human		name
127295396	CV1112232	single nucleotide variant	NM_212482.4(FN1):c.4161C>A (p.Thr1387=)	Glomerulopathy with fibronectin deposits 2 [RCV002501589]\|not provided [RCV001452500]	likely benign	2	215391723	215391723	Human	1	name
127327222	CV1112233	single nucleotide variant	NM_212482.4(FN1):c.3867G>A (p.Pro1289=)	not provided [RCV001469007]	likely benign	2	215393133	215393133	Human		name
127309833	CV1112236	single nucleotide variant	NM_212482.4(FN1):c.887C>T (p.Pro296Leu)	not provided [RCV001456450]	benign\|likely benign	2	215425243	215425243	Human		name
127322765	CV1133143	single nucleotide variant	NM_212482.4(FN1):c.6915T>C (p.His2305=)	not provided [RCV001485025]	likely benign	2	215367966	215367966	Human		name
127332092	CV1133144	single nucleotide variant	NM_212482.4(FN1):c.4719C>T (p.Tyr1573=)	Glomerulopathy with fibronectin deposits 2 [RCV002488289]\|not provided [RCV001489266]	likely benign	2	215384870	215384870	Human	1	name
127317945	CV1133145	single nucleotide variant	NM_212482.4(FN1):c.3243C>A (p.Val1081=)	not provided [RCV001503527]	likely benign	2	215404399	215404399	Human		name
127317266	CV1153966	single nucleotide variant	NM_212482.4(FN1):c.7368T>G (p.Val2456=)	not provided [RCV001520988]	benign	2	215361621	215361621	Human		name
127318857	CV1153967	single nucleotide variant	NM_212482.4(FN1):c.7161T>C (p.Tyr2387=)	Glomerulopathy with fibronectin deposits 2 [RCV001702111]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702905]\|not provided [RCV001521850]	benign	2	215364969	215364969	Human	2	name
127304048	CV1153972	single nucleotide variant	NM_212482.4(FN1):c.5964C>T (p.Ile1988=)	Glomerulopathy with fibronectin deposits 2 [RCV002495803]\|not provided [RCV001515743]	benign\|likely benign	2	215375642	215375642	Human	1	name
127299074	CV1153973	single nucleotide variant	NM_212482.4(FN1):c.5691A>T (p.Gly1897=)	Glomerulopathy with fibronectin deposits 2 [RCV001703103]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702899]\|not provided [RCV001513542]	benign	2	215378194	215378194	Human	2	name
127318871	CV1153976	single nucleotide variant	NM_212482.4(FN1):c.4725G>A (p.Glu1575=)	Glomerulopathy with fibronectin deposits 2 [RCV001702906]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702907]\|not provided [RCV001521853]	benign	2	215384864	215384864	Human	2	name
127291422	CV1153977	single nucleotide variant	NM_212482.4(FN1):c.3156A>C (p.Pro1052=)	Glomerulopathy with fibronectin deposits 2 [RCV001702897]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001703100]\|not provided [RCV001510357]	benign	2	215404486	215404486	Human	2	name
127291426	CV1153978	single nucleotide variant	NM_212482.4(FN1):c.3111A>C (p.Gly1037=)	Glomerulopathy with fibronectin deposits 2 [RCV001702598]\|Spondylometaphyseal dysplasia - Sutcliffe type [RCV001702898]\|not provided [RCV001510358]	benign	2	215404531	215404531	Human	2	name
150555959	CV1305465	single nucleotide variant	NM_212482.4(FN1):c.697G>C (p.Asp233His)	not provided [RCV001773398]	uncertain significance	2	215428327	215428327	Human		name
151858030	CV1347560	single nucleotide variant	NM_212482.4(FN1):c.692G>A (p.Cys231Tyr)	not provided [RCV002034022]	uncertain significance	2	215428332	215428332	Human		name
151737031	CV1391609	single nucleotide variant	NM_212482.4(FN1):c.749A>C (p.Asp250Ala)	Glomerulopathy with fibronectin deposits 2 [RCV002482414]\|not provided [RCV002041828]	uncertain significance	2	215428275	215428275	Human	1	name
151807230	CV1417655	single nucleotide variant	NM_212482.4(FN1):c.665G>A (p.Arg222His)	Glomerulopathy with fibronectin deposits 2 [RCV002506922]\|not provided [RCV001867664]	likely benign\|uncertain significance	2	215430735	215430735	Human	1	name
151880796	CV1421587	single nucleotide variant	NM_212482.4(FN1):c.872C>A (p.Ala291Glu)	not provided [RCV001886451]	uncertain significance	2	215425258	215425258	Human		name
151817402	CV1427413	single nucleotide variant	NM_212482.4(FN1):c.587T>A (p.Val196Glu)	Glomerulopathy with fibronectin deposits 2 [RCV005014742]\|Inborn genetic diseases [RCV004980826]\|not provided [RCV001878883]	likely benign\|uncertain significance	2	215430813	215430813	Human	2	name
151709797	CV1433343	single nucleotide variant	NM_212482.4(FN1):c.340C>T (p.Arg114Cys)	not provided [RCV002001717]	uncertain significance	2	215433399	215433399	Human		name
151886495	CV1435741	single nucleotide variant	NM_212482.4(FN1):c.712A>T (p.Thr238Ser)	not provided [RCV001962772]	uncertain significance	2	215428312	215428312	Human		name
151842073	CV1436066	single nucleotide variant	NM_212482.4(FN1):c.746A>C (p.Lys249Thr)	not provided [RCV001956879]	uncertain significance	2	215428278	215428278	Human		name
151795391	CV1437626	single nucleotide variant	NM_212482.4(FN1):c.755G>A (p.Arg252Gln)	not provided [RCV001876892]	uncertain significance	2	215428269	215428269	Human		name
151711341	CV1440027	single nucleotide variant	NM_212482.4(FN1):c.907C>T (p.Pro303Ser)	Glomerulopathy with fibronectin deposits 2 [RCV002482586]\|not provided [RCV001908072]	uncertain significance	2	215425223	215425223	Human	1	name
151851737	CV1458867	single nucleotide variant	NM_212482.4(FN1):c.592G>A (p.Gly198Arg)	Glomerulopathy with fibronectin deposits 2 [RCV002507797]\|Inborn genetic diseases [RCV002548752]\|not provided [RCV002016678]	uncertain significance	2	215430808	215430808	Human	2	name
151736338	CV1465982	single nucleotide variant	NM_212482.4(FN1):c.604G>A (p.Glu202Lys)	Inborn genetic diseases [RCV005341069]\|not provided [RCV002041756]	likely benign\|uncertain significance	2	215430796	215430796	Human	1	name
151730968	CV1489643	single nucleotide variant	NM_212482.4(FN1):c.864T>G (p.Asp288Glu)	Glomerulopathy with fibronectin deposits 2 [RCV005016757]\|not provided [RCV001910866]	uncertain significance	2	215425266	215425266	Human	1	name
151764995	CV1491061	single nucleotide variant	NM_212482.4(FN1):c.3447C>T (p.Tyr1149=)	not provided [RCV001949582]	likely benign	2	215397750	215397750	Human		name
151892561	CV1493651	single nucleotide variant	NM_212482.4(FN1):c.790G>A (p.Gly264Ser)	Glomerulopathy with fibronectin deposits 2 [RCV002484644]\|not provided [RCV001944241]	uncertain significance	2	215428234	215428234	Human	1	name
152108302	CV1519995	single nucleotide variant	NM_212482.4(FN1):c.4842C>T (p.Gly1614=)	not provided [RCV002134150]	likely benign	2	215384072	215384072	Human		name
152120844	CV1521352	single nucleotide variant	NM_212482.4(FN1):c.4296C>A (p.Val1432=)	not provided [RCV002135689]	likely benign	2	215388258	215388258	Human		name
152044844	CV1525636	single nucleotide variant	NM_212482.4(FN1):c.6090G>A (p.Lys2030=)	not provided [RCV002126538]	likely benign	2	215375281	215375281	Human		name
152050557	CV1533184	single nucleotide variant	NM_212482.4(FN1):c.5920C>T (p.Leu1974=)	not provided [RCV002166823]	likely benign	2	215375686	215375686	Human		name
152030418	CV1534208	single nucleotide variant	NM_212482.4(FN1):c.6507G>A (p.Pro2169=)	Glomerulopathy with fibronectin deposits 2 [RCV002494178]\|not provided [RCV002086131]	likely benign	2	215372116	215372116	Human	1	name
152031728	CV1546109	single nucleotide variant	NM_212482.4(FN1):c.6336T>C (p.Pro2112=)	Glomerulopathy with fibronectin deposits 2 [RCV002500044]\|not provided [RCV002124618]	benign\|likely benign	2	215372287	215372287	Human	1	name
152071227	CV1549057	single nucleotide variant	NM_212482.4(FN1):c.5127C>T (p.Ser1709=)	not provided [RCV002091615]	likely benign	2	215382249	215382249	Human		name
152041137	CV1553464	single nucleotide variant	NM_212482.4(FN1):c.6459G>A (p.Pro2153=)	Glomerulopathy with fibronectin deposits 2 [RCV002479893]\|not provided [RCV002087978]	likely benign	2	215372164	215372164	Human	1	name
152105593	CV1559944	single nucleotide variant	NM_212482.4(FN1):c.6639A>G (p.Ser2213=)	not provided [RCV002133808]	likely benign	2	215371984	215371984	Human		name
152106415	CV1560081	single nucleotide variant	NM_212482.4(FN1):c.3909T>G (p.Val1303=)	Glomerulopathy with fibronectin deposits 2 [RCV002500256]\|not provided [RCV002133908]	likely benign	2	215393091	215393091	Human	1	name
152116437	CV1566938	single nucleotide variant	NM_212482.4(FN1):c.5943T>C (p.Ala1981=)	Glomerulopathy with fibronectin deposits 2 [RCV002507953]\|not provided [RCV002097553]	likely benign	2	215375663	215375663	Human	1	name
152100604	CV1578769	single nucleotide variant	NM_212482.4(FN1):c.5907C>T (p.Asp1969=)	not provided [RCV002151766]	likely benign	2	215375699	215375699	Human		name
152025984	CV1586671	single nucleotide variant	NM_212482.4(FN1):c.6066C>T (p.Thr2022=)	Glomerulopathy with fibronectin deposits 2 [RCV002494077]\|not provided [RCV002185001]	likely benign	2	215375305	215375305	Human	1	name
152136468	CV1587879	single nucleotide variant	NM_212482.4(FN1):c.5496G>A (p.Gln1832=)	not provided [RCV002083574]	likely benign	2	215379256	215379256	Human		name
152087746	CV1601313	single nucleotide variant	NM_212482.4(FN1):c.6576C>T (p.His2192=)	not provided [RCV002093735]	likely benign	2	215372047	215372047	Human		name
152036854	CV1605432	single nucleotide variant	NM_212482.4(FN1):c.3150G>A (p.Lys1050=)	not provided [RCV002087356]	likely benign	2	215404492	215404492	Human		name
152106885	CV1612911	single nucleotide variant	NM_212482.4(FN1):c.5511T>C (p.Asn1837=)	Glomerulopathy with fibronectin deposits 2 [RCV002500105]\|not provided [RCV002173829]	likely benign	2	215379241	215379241	Human	1	name
152027302	CV1626858	single nucleotide variant	NM_212482.4(FN1):c.7116C>T (p.Asn2372=)	Glomerulopathy with fibronectin deposits 2 [RCV002494089]\|not provided [RCV002185451]	likely benign	2	215365533	215365533	Human	1	name
152047979	CV1627474	single nucleotide variant	NM_212482.4(FN1):c.3006C>T (p.Asn1002=)	not provided [RCV002108575]	likely benign	2	215404636	215404636	Human		name
152027271	CV1636148	single nucleotide variant	NM_212482.4(FN1):c.3198C>T (p.Leu1066=)	not provided [RCV002085078]	likely benign	2	215404444	215404444	Human		name
152108468	CV1648278	single nucleotide variant	NM_212482.4(FN1):c.6921C>T (p.Ala2307=)	not provided [RCV002116229]	likely benign	2	215367960	215367960	Human		name
152074968	CV1652859	single nucleotide variant	NM_212482.4(FN1):c.4767G>C (p.Gly1589=)	not provided [RCV002148579]	likely benign	2	215384147	215384147	Human		name
155748983	CV1779030	single nucleotide variant	NM_212482.4(FN1):c.811G>A (p.Glu271Lys)	not provided [RCV002304132]	uncertain significance	2	215428213	215428213	Human		name
155947215	CV1921684	single nucleotide variant	NM_212482.4(FN1):c.4524C>T (p.Asn1508=)	not provided [RCV002616014]	likely benign	2	215386777	215386777	Human		name
155978697	CV1972296	single nucleotide variant	NM_212482.4(FN1):c.4053A>G (p.Thr1351=)	not provided [RCV002617500]	likely benign	2	215392947	215392947	Human		name
155912677	CV1980300	single nucleotide variant	NM_212482.4(FN1):c.5013T>C (p.Asn1671=)	not provided [RCV002614104]	likely benign	2	215383365	215383365	Human		name
155941393	CV2006256	single nucleotide variant	NM_133372.3(FNIP1):c.903A>G (p.Val301=)	not provided [RCV002685485]	likely benign	5	131706422	131706422	Human		name
155958630	CV2010625	single nucleotide variant	NM_212482.4(FN1):c.5637T>C (p.Tyr1879=)	not provided [RCV002686403]	likely benign	2	215378248	215378248	Human		name
155974366	CV2021982	single nucleotide variant	NM_212482.4(FN1):c.5391C>T (p.His1797=)	Glomerulopathy with fibronectin deposits 2 [RCV005019350]\|not provided [RCV002755035]	likely benign\|uncertain significance	2	215380854	215380854	Human	1	name
155954706	CV2086884	single nucleotide variant	NM_212482.4(FN1):c.6123G>A (p.Arg2041=)	not provided [RCV002862536]	likely benign	2	215375248	215375248	Human		name
155948688	CV2087860	single nucleotide variant	NM_212482.4(FN1):c.4746C>T (p.Val1582=)	not provided [RCV002880376]	likely benign	2	215384168	215384168	Human		name
155993449	CV2095609	single nucleotide variant	NM_212482.4(FN1):c.6615A>G (p.Glu2205=)	not provided [RCV002908270]	likely benign	2	215372008	215372008	Human		name
155996247	CV2109408	single nucleotide variant	NM_212482.4(FN1):c.3324G>A (p.Thr1108=)	not provided [RCV002947573]	likely benign	2	215399281	215399281	Human		name
155979131	CV2157133	single nucleotide variant	NM_212482.4(FN1):c.687T>G (p.Asn229Lys)	not provided [RCV003016289]	uncertain significance	2	215428337	215428337	Human		name
155952446	CV2161364	single nucleotide variant	NM_212482.4(FN1):c.5340G>A (p.Leu1780=)	not provided [RCV003032510]	likely benign	2	215380905	215380905	Human		name
155927534	CV2218405	single nucleotide variant	NM_022158.4(FN3K):c.245G>A (p.Gly82Asp)	not specified [RCV004090699]	uncertain significance	17	82738592	82738592	Human		name
12741239	CV359346	single nucleotide variant	NM_212482.4(FN1):c.976C>T (p.Gln326Ter)	not provided [RCV000414499]	uncertain significance	2	215425154	215425154	Human		name
12893964	CV405614	single nucleotide variant	NM_212482.4(FN1):c.693C>G (p.Cys231Trp)	Spondylometaphyseal dysplasia [RCV000754912]\|not provided [RCV000480973]	likely pathogenic	2	215428331	215428331	Human	2	name
13442861	CV411545	single nucleotide variant	NM_212482.4(FN1):c.778T>G (p.Cys260Gly)	Spondylometaphyseal dysplasia - Sutcliffe type [RCV000755747]\|Spondylometaphyseal dysplasia [RCV000509583]	likely pathogenic	2	215428246	215428246	Human	3	name
13442865	CV411546	single nucleotide variant	NM_212482.4(FN1):c.718T>G (p.Tyr240Asp)	Spondylometaphyseal dysplasia - Sutcliffe type [RCV000570760]\|Spondylometaphyseal dysplasia [RCV000509587]	pathogenic\|likely pathogenic	2	215428306	215428306	Human	3	name
13442863	CV411547	single nucleotide variant	NM_212482.4(FN1):c.675C>G (p.Cys225Trp)	Spondylometaphyseal dysplasia - Sutcliffe type [RCV000755737]\|Spondylometaphyseal dysplasia [RCV000509585]\|not provided [RCV003558392]	pathogenic\|likely pathogenic	2	215430725	215430725	Human	3	name
13442860	CV411548	single nucleotide variant	NM_212482.4(FN1):c.367T>C (p.Cys123Arg)	Spondylometaphyseal dysplasia - Sutcliffe type [RCV000575065]\|Spondylometaphyseal dysplasia [RCV000509582]\|not provided [RCV002526994]	pathogenic\|likely pathogenic	2	215433372	215433372	Human	3	name
13472316	CV443163	single nucleotide variant	NM_212482.4(FN1):c.773G>A (p.Cys258Tyr)	Spondylometaphyseal dysplasia [RCV000754913]\|not provided [RCV000519100]	likely pathogenic\|uncertain significance	2	215428251	215428251	Human	2	name
14392988	CV540474	single nucleotide variant	NM_212482.4(FN1):c.638G>A (p.Cys213Tyr)	Spondylometaphyseal dysplasia [RCV000754909]\|not provided [RCV001796767]	pathogenic\|likely pathogenic\|uncertain significance	2	215430762	215430762	Human	2	name
14392990	CV540475	single nucleotide variant	NM_212482.4(FN1):c.506G>A (p.Cys169Tyr)	Spondylometaphyseal dysplasia [RCV000754911]	likely pathogenic	2	215431874	215431874	Human	2	name
14392989	CV540476	single nucleotide variant	NM_212482.4(FN1):c.368G>A (p.Cys123Tyr)	Spondylometaphyseal dysplasia [RCV000754910]	likely pathogenic	2	215433371	215433371	Human	2	name
14397155	CV612596	single nucleotide variant	NM_212482.4(FN1):c.3972A>C (p.Thr1324=)	not provided [RCV000762319]	uncertain significance	2	215393028	215393028	Human		name
15193197	CV697299	single nucleotide variant	NM_212482.4(FN1):c.4791C>T (p.Ser1597=)	Glomerulopathy with fibronectin deposits 2 [RCV002489326]\|not provided [RCV000955301]	benign\|likely benign	2	215384123	215384123	Human	1	name
15156310	CV697301	single nucleotide variant	NM_212482.4(FN1):c.4146A>G (p.Pro1382=)	Glomerulopathy with fibronectin deposits 2 [RCV002479089]\|not provided [RCV000946672]	benign\|likely benign	2	215391738	215391738	Human	1	name
15156317	CV697302	single nucleotide variant	NM_212482.4(FN1):c.3837C>T (p.Thr1279=)	not provided [RCV000946673]	benign\|likely benign	2	215393163	215393163	Human		name
15173730	CV708008	single nucleotide variant	NM_212482.4(FN1):c.7182C>T (p.His2394=)	not provided [RCV000972642]	benign	2	215364948	215364948	Human		name
15156707	CV708011	single nucleotide variant	NM_212482.4(FN1):c.3189C>T (p.Thr1063=)	Glomerulopathy with fibronectin deposits 2 [RCV002489404]\|not provided [RCV000969166]	benign\|likely benign	2	215404453	215404453	Human	1	name
15161789	CV710296	single nucleotide variant	NM_032532.3(FNDC1):c.927G>A (p.Arg309=)	not provided [RCV000970152]	benign	6	159225577	159225577	Human		name
15134144	CV711543	single nucleotide variant	NM_002027.3(FNTA):c.190G>A (p.Val64Ile)	not provided [RCV000965076]	benign	8	43056536	43056536	Human		name
15168339	CV719600	single nucleotide variant	NM_212482.4(FN1):c.313A>C (p.Thr105Pro)	not provided [RCV000883043]	benign	2	215433426	215433426	Human		name
15176653	CV721845	single nucleotide variant	NM_032532.3(FNDC1):c.651C>T (p.His217=)	not provided [RCV000884631]	benign	6	159215135	159215135	Human		name
15156630	CV724475	single nucleotide variant	NM_015308.5(FNBP4):c.684G>T (p.Thr228=)	not provided [RCV000880668]	likely benign	11	47751244	47751244	Human		name
15187848	CV733143	single nucleotide variant	NM_212482.4(FN1):c.5964C>A (p.Ile1988=)	not provided [RCV000909202]	likely benign	2	215375642	215375642	Human		name
15185710	CV733146	single nucleotide variant	NM_212482.4(FN1):c.4164C>T (p.Asn1388=)	not provided [RCV000908603]	benign	2	215391720	215391720	Human		name
15182448	CV733148	single nucleotide variant	NM_212482.4(FN1):c.3012G>A (p.Gln1004=)	Glomerulopathy with fibronectin deposits 2 [RCV002487979]\|not provided [RCV000907823]	likely benign	2	215404630	215404630	Human	1	name
15097803	CV747263	single nucleotide variant	NM_212482.4(FN1):c.7209T>C (p.Tyr2403=)	not provided [RCV000914094]	likely benign	2	215364921	215364921	Human		name
15152671	CV747264	single nucleotide variant	NM_212482.4(FN1):c.6840C>T (p.Thr2280=)	not provided [RCV000923917]	likely benign	2	215370307	215370307	Human		name
15203330	CV747265	single nucleotide variant	NM_212482.4(FN1):c.6639A>C (p.Ser2213=)	not provided [RCV000913874]	likely benign	2	215371984	215371984	Human		name
15111453	CV747266	single nucleotide variant	NM_212482.4(FN1):c.6600C>T (p.Ala2200=)	not provided [RCV000916733]	likely benign	2	215372023	215372023	Human		name
15107423	CV747267	single nucleotide variant	NM_212482.4(FN1):c.6537C>T (p.His2179=)	not provided [RCV000915952]	likely benign	2	215372086	215372086	Human		name
15201984	CV747268	single nucleotide variant	NM_212482.4(FN1):c.6249C>T (p.Asp2083=)	not provided [RCV000913304]	likely benign	2	215372374	215372374	Human		name
15203375	CV747269	single nucleotide variant	NM_212482.4(FN1):c.5649C>G (p.Val1883=)	not provided [RCV000913924]	likely benign	2	215378236	215378236	Human		name
15203363	CV747270	single nucleotide variant	NM_212482.4(FN1):c.4056G>A (p.Leu1352=)	not provided [RCV000913909]	likely benign	2	215392944	215392944	Human		name
15123480	CV747272	single nucleotide variant	NM_212482.4(FN1):c.3090C>T (p.Thr1030=)	not provided [RCV000918829]	likely benign	2	215404552	215404552	Human		name
15180841	CV762887	single nucleotide variant	NM_212482.4(FN1):c.4626G>A (p.Pro1542=)	Glomerulopathy with fibronectin deposits 2 [RCV002505380]\|not provided [RCV000929984]	likely benign	2	215384963	215384963	Human	1	name
15177338	CV762894	single nucleotide variant	NM_212482.4(FN1):c.904C>G (p.Pro302Ala)	Inborn genetic diseases [RCV004619457]\|not provided [RCV000929131]	likely benign	2	215425226	215425226	Human	1	name
126754707	CV988358	single nucleotide variant	NM_212482.4(FN1):c.860C>T (p.Thr287Ile)	Glomerulopathy with fibronectin deposits 2 [RCV005029868]\|not provided [RCV001298185]	uncertain significance	2	215425270	215425270	Human	1	name

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