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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HGVS dbSNP
NM_002977.3(SCN9A):c.2567G>A (p.Gly856Asp) rs879254102
NM_002977.3(SCN9A):c.2686C>T (p.Arg896Trp) rs202152511
NM_002977.3(SCN9A):c.4474A>T (p.Lys1492Ter) rs876661206
NM_002977.3(SCN9A):c.4835T>C (p.Leu1612Pro) rs1131691776
NM_002977.3(SCN9A):c.5359G>T (p.Glu1787Ter) rs770416478
NM_002977.3(SCN9A):c.5536del (p.Asp1846fs) rs1553472910

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