ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as uncertain significance by Athena Diagnostics Inc

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Total variants: 9
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HGVS dbSNP
NM_001365536.1(SCN9A):c.1109C>T (p.Thr370Met) rs200391162
NM_001365536.1(SCN9A):c.1150G>A (p.Val384Ile) rs200973534
NM_001365536.1(SCN9A):c.2644G>C (p.Val882Leu) rs1553487882
NM_001365536.1(SCN9A):c.3271A>G (p.Ile1091Val) rs202212176
NM_001365536.1(SCN9A):c.3509T>C (p.Ile1170Thr) rs73019664
NM_001365536.1(SCN9A):c.3538A>G (p.Asn1180Asp) rs750269576
NM_001365536.1(SCN9A):c.5030A>T (p.Asp1677Val) rs1553473210
NM_001365536.1(SCN9A):c.5425C>G (p.Leu1809Val) rs199954555
NM_001365536.1(SCN9A):c.5791G>C (p.Asp1931His) rs200410805

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