ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as likely benign for not specified

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_001365536.1(SCN9A):c.1287T>A (p.Arg429=) rs6747673 0.56670
NM_001365536.1(SCN9A):c.1266A>G (p.Glu422=) rs13402180 0.38348
NM_001365536.1(SCN9A):c.1119T>C (p.Ala373=) rs13414203 0.38341
NM_001365536.1(SCN9A):c.3802-4A>G rs75230218 0.06754
NM_001365536.1(SCN9A):c.4812G>T (p.Val1604=) rs149207258 0.06646
NM_001365536.1(SCN9A):c.1469G>A (p.Ser490Asn) rs58022607 0.04393
NM_001365536.1(SCN9A):c.1155G>T (p.Val385=) rs58465962 0.04390
NM_001365536.1(SCN9A):c.5756A>G (p.Asp1919Gly) rs3750904 0.02756
NM_001365536.1(SCN9A):c.3802-8T>C rs76550960 0.02262
NM_001365536.1(SCN9A):c.3362G>A (p.Arg1121Gln) rs74401238 0.02210
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu) rs12478318 0.01339
NM_001365536.1(SCN9A):c.3004G>T (p.Val1002Leu) rs4369876 0.01322
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser) rs141268327 0.00496
NM_001365536.1(SCN9A):c.2190G>C (p.Trp730Cys) rs202055175 0.00341
NM_001365536.1(SCN9A):c.3361C>T (p.Arg1121Trp) rs190664764 0.00304
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val) rs182650126 0.00278
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg) rs121908919 0.00180
NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val) rs180922748 0.00174
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg) rs202084411 0.00173
NM_001365536.1(SCN9A):c.4314C>T (p.Val1438=) rs188336294 0.00171
NM_001365536.1(SCN9A):c.3675C>A (p.Ile1225=) rs77144869 0.00141
NM_001365536.1(SCN9A):c.2409T>C (p.Tyr803=) rs142219317 0.00106
NM_001365536.1(SCN9A):c.1326G>A (p.Ala442=) rs200065104 0.00102
NM_001365536.1(SCN9A):c.3195C>T (p.Ser1065=) rs111674454 0.00099
NM_001365536.1(SCN9A):c.2766C>T (p.Arg922=) rs199653503 0.00096
NM_001365536.1(SCN9A):c.3020G>A (p.Arg1007His) rs188145203 0.00077
NM_001365536.1(SCN9A):c.4315G>A (p.Val1439Ile) rs149346064 0.00061
NM_001365536.1(SCN9A):c.3002A>G (p.Tyr1001Cys) rs199692186 0.00056
NM_001365536.1(SCN9A):c.3402G>T (p.Leu1134Phe) rs200160858 0.00052
NM_001365536.1(SCN9A):c.4923T>C (p.Leu1641=) rs199550149 0.00041
NM_001365536.1(SCN9A):c.2192T>A (p.Ile731Lys) rs200945460 0.00019
NM_001365536.1(SCN9A):c.1177C>T (p.Leu393=) rs184773311 0.00017
NM_001365536.1(SCN9A):c.3573C>T (p.His1191=) rs375710841 0.00016
NM_001365536.1(SCN9A):c.965+13T>C rs772337722 0.00010
NM_001365536.1(SCN9A):c.2634C>T (p.Phe878=) rs188678956 0.00007
NM_001365536.1(SCN9A):c.3802-13del rs747729984 0.00007
NM_001365536.1(SCN9A):c.5945A>T (p.Asp1982Val) rs199822303 0.00006
NM_001365536.1(SCN9A):c.1975-8T>A rs752961542 0.00005
NM_001365536.1(SCN9A):c.3540C>T (p.Asn1180=) rs766241126 0.00003
NM_001365536.1(SCN9A):c.966-8G>A rs199942413 0.00003
NM_001365536.1(SCN9A):c.1602+15G>T rs201987507 0.00002
NM_001365536.1(SCN9A):c.1107+7A>G rs199623041 0.00001
NM_001365536.1(SCN9A):c.2253C>T (p.Thr751=) rs751536693 0.00001
NM_001365536.1(SCN9A):c.2712G>A (p.Thr904=) rs200494981 0.00001
NM_001365536.1(SCN9A):c.3036A>G (p.Lys1012=) rs200375962 0.00001
NM_001365536.1(SCN9A):c.3807T>A (p.Ser1269=) rs1272510761 0.00001
NM_001365536.1(SCN9A):c.990T>C (p.Cys330=) rs1384436013 0.00001
NM_001365536.1(SCN9A):c.1828C>A (p.Pro610Thr) rs41268673
NM_001365536.1(SCN9A):c.2420G>T (p.Gly807Val) rs1553488264
NM_001365536.1(SCN9A):c.2874+11_2874+13delinsTT rs1553487749
NM_001365536.1(SCN9A):c.2875-18C>T rs1553486847
NM_001365536.1(SCN9A):c.3003T>C (p.Tyr1001=) rs886038521
NM_001365536.1(SCN9A):c.3351+15T>C rs763278343
NM_001365536.1(SCN9A):c.3834T>G (p.Leu1278=) rs1553480111
NM_001365536.1(SCN9A):c.3925-10T>C
NM_001365536.1(SCN9A):c.4141C>A (p.Arg1381=) rs748159444
NM_001365536.1(SCN9A):c.5028T>C (p.Asn1676=) rs1553473212
NM_001365536.1(SCN9A):c.965+18T>C rs1553492740

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