ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as likely benign for Indifference to pain, congenital, autosomal recessive

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Total variants: 25
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HGVS dbSNP
NM_001365536.1(SCN9A):c.*2212T>C rs200750861
NM_001365536.1(SCN9A):c.*2312A>T rs185580193
NM_001365536.1(SCN9A):c.*2721C>G rs199595958
NM_001365536.1(SCN9A):c.*3038C>T rs115766730
NM_001365536.1(SCN9A):c.*3317A>G rs191667986
NM_001365536.1(SCN9A):c.*362C>T
NM_001365536.1(SCN9A):c.*920T>A rs201424899
NM_001365536.1(SCN9A):c.1398C>T (p.Ser466=) rs201531206
NM_001365536.1(SCN9A):c.1555G>A (p.Glu519Lys) rs187453572
NM_001365536.1(SCN9A):c.1838C>T (p.Pro613Leu) rs200671761
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg) rs121908919
NM_001365536.1(SCN9A):c.2190G>C (p.Trp730Cys) rs202055175
NM_001365536.1(SCN9A):c.2192T>A (p.Ile731Lys) rs200945460
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val) rs182650126
NM_001365536.1(SCN9A):c.2517+6C>T rs145316463
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu) rs12478318
NM_001365536.1(SCN9A):c.2875-6A>G rs760470229
NM_001365536.1(SCN9A):c.3472+14T>C rs201979079
NM_001365536.1(SCN9A):c.3767A>G (p.Asn1256Ser) rs141268327
NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val) rs180922748
NM_001365536.1(SCN9A):c.4315G>A (p.Val1439Ile) rs149346064
NM_001365536.1(SCN9A):c.4495C>A (p.Arg1499=) rs187558439
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg) rs202084411
NM_001365536.1(SCN9A):c.5711G>A (p.Arg1904His) rs79805025
NM_001365536.1(SCN9A):c.5779C>T (p.Leu1927Phe) rs111558968

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