ClinVar Miner

List of variants in gene SCN9A reported as uncertain significance by GeneDx

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_001365536.1(SCN9A):c.684C>G (p.Ile228Met) rs71428908 0.00081
NM_001365536.1(SCN9A):c.361A>C (p.Lys121Gln) rs200486515 0.00009
NM_001365536.1(SCN9A):c.641G>A (p.Arg214Gln) rs201741634 0.00006
NM_001365536.1(SCN9A):c.764G>A (p.Cys255Tyr) rs755139637 0.00005
NM_001365536.1(SCN9A):c.76C>T (p.Arg26Cys) rs199933920 0.00005
NM_001365536.1(SCN9A):c.184A>G (p.Ile62Val) rs121908920 0.00004
NM_001365536.1(SCN9A):c.118A>G (p.Lys40Glu) rs371565974 0.00003
NM_001365536.1(SCN9A):c.136G>A (p.Ala46Thr) rs779344629 0.00002
NM_001365536.1(SCN9A):c.294C>A (p.Phe98Leu) rs199824489 0.00002
NM_001365536.1(SCN9A):c.262T>C (p.Phe88Leu) rs1012999498 0.00001
NM_001365536.1(SCN9A):c.304G>T (p.Ala102Ser) rs201343843 0.00001
NM_001365536.1(SCN9A):c.628G>A (p.Val210Ile) rs200619065 0.00001
NM_001365536.1(SCN9A):c.892G>A (p.Asp298Asn) rs1057518384 0.00001
NM_001365536.1(SCN9A):c.153T>A (p.Ser51Arg) rs199836776
NM_001365536.1(SCN9A):c.20C>G (p.Pro7Arg) rs773012423
NM_001365536.1(SCN9A):c.267A>C (p.Ile89=) rs200809157
NM_001365536.1(SCN9A):c.431C>T (p.Thr144Ile) rs748032198
NM_001365536.1(SCN9A):c.488A>G (p.Tyr163Cys) rs876661294
NM_001365536.1(SCN9A):c.660A>C (p.Arg220Ser)
NM_001365536.1(SCN9A):c.695A>G (p.Lys232Arg) rs879253936
NM_001365536.1(SCN9A):c.713T>C (p.Leu238Ser) rs1553495258
NM_001365536.1(SCN9A):c.817C>T (p.His273Tyr)
NM_001365536.1(SCN9A):c.847A>T (p.Asn283Tyr) rs1553495127

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