ClinVar Miner

List of variants in gene SCN9A reported as likely benign for Severe myoclonic epilepsy in infancy

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Total variants: 6
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HGVS dbSNP
NM_002977.3(SCN9A):c.-277C>T rs201445594
NM_002977.3(SCN9A):c.-283G>C rs191091185
NM_002977.3(SCN9A):c.-294T>C rs141521157
NM_002977.3(SCN9A):c.129T>C (p.Asp43=) rs200826539
NM_002977.3(SCN9A):c.29A>G (p.Gln10Arg) rs267607030
NM_002977.3(SCN9A):c.554G>A (p.Arg185His) rs73969684

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