ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_001365536.1(SCN9A):c.1469G>A (p.Ser490Asn) rs58022607 0.04393
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu) rs12478318 0.01480
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.2248A>G (p.Ile750Val) rs182650126 0.00270
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg) rs202084411 0.00190
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg) rs121908919 0.00176
NM_001365536.1(SCN9A):c.4314C>T (p.Val1438=) rs188336294 0.00171
NM_001365536.1(SCN9A):c.3051G>C (p.Lys1017Asn) rs147623238 0.00144
NM_001365536.1(SCN9A):c.3509T>C (p.Ile1170Thr) rs73019664 0.00128
NM_001365536.1(SCN9A):c.3195C>T (p.Ser1065=) rs111674454 0.00096
NM_001365536.1(SCN9A):c.1326G>A (p.Ala442=) rs200065104 0.00092
NM_001365536.1(SCN9A):c.1464C>T (p.Leu488=) rs200682458 0.00058
NM_001365536.1(SCN9A):c.3402G>T (p.Leu1134Phe) rs200160858 0.00052
NM_001365536.1(SCN9A):c.3002A>G (p.Tyr1001Cys) rs199692186 0.00048
NM_001365536.1(SCN9A):c.4495C>A (p.Arg1499=) rs187558439 0.00019
NM_001365536.1(SCN9A):c.1177C>T (p.Leu393=) rs184773311 0.00018
NM_001365536.1(SCN9A):c.1110G>A (p.Thr370=) rs202002028 0.00016
NM_001365536.1(SCN9A):c.3228T>A (p.Gly1076=) rs200393050 0.00013
NM_001365536.1(SCN9A):c.3207C>T (p.His1069=) rs200689065 0.00010
NM_001365536.1(SCN9A):c.2165T>C (p.Leu722Ser) rs187526567 0.00009
NM_001365536.1(SCN9A):c.3975A>G (p.Leu1325=) rs199988325 0.00009
NM_001365536.1(SCN9A):c.4767C>T (p.Ser1589=) rs200690956 0.00003
NM_001365536.1(SCN9A):c.1107+7A>G rs199623041 0.00001
NM_001365536.1(SCN9A):c.1158T>A (p.Ile386=) rs200963646 0.00001
NM_001365536.1(SCN9A):c.1347T>C (p.Ser449=) rs201990547 0.00001
NM_001365536.1(SCN9A):c.1566G>A (p.Arg522=) rs1340370507 0.00001
NM_001365536.1(SCN9A):c.4503+8A>T rs753899025 0.00001
NM_001365536.1(SCN9A):c.1314+5T>C rs770452089
NM_001365536.1(SCN9A):c.1974+9_1974+15del rs771477692
NM_001365536.1(SCN9A):c.2874+11_2874+13delinsTT rs1553487749
NM_001365536.1(SCN9A):c.3003T>C (p.Tyr1001=) rs886038521
NM_001365536.1(SCN9A):c.3180T>C (p.Ser1060=) rs199697334

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