ClinVar Miner

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

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Total variants: 3
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NM_001365536.1(SCN9A):c.*2616_*2626del rs145255931
NM_001365536.1(SCN9A):c.*798dup rs564394161
NM_001365536.1(SCN9A):c.1975-12dup rs35888674

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