ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as likely pathogenic for not provided

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Total variants: 6
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NM_001365536.1(SCN9A):c.2600G>A (p.Gly867Asp) rs879254102
NM_001365536.1(SCN9A):c.2719C>T (p.Arg907Trp) rs202152511
NM_001365536.1(SCN9A):c.4507A>T (p.Lys1503Ter) rs876661206
NM_001365536.1(SCN9A):c.4868T>C (p.Leu1623Pro) rs1131691776
NM_001365536.1(SCN9A):c.5392G>T (p.Glu1798Ter) rs770416478
NM_001365536.1(SCN9A):c.5569del (p.Asp1857fs) rs1553472910

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