ClinVar Miner

List of variants reported as likely pathogenic for Benign familial neonatal-infantile seizures

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Total variants: 3
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HGVS dbSNP
NC_000002.11:g.(?_166152283)_(166246384_?)dup
NM_001040142.2(SCN2A):c.5117G>C (p.Cys1706Ser) rs1553463513
NM_001040142.2(SCN2A):c.5551C>T (p.Arg1851Trp) rs1553463718

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