ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as likely benign for Severe myoclonic epilepsy in infancy

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Total variants: 4
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NM_001365536.1(SCN9A):c.*1605_*1606del rs200091138
NM_001365536.1(SCN9A):c.*1960_*1962dup rs202073550
NM_001365536.1(SCN9A):c.1975-3del rs35888674
NM_001365536.1(SCN9A):c.2875-5del rs774840081

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