ClinVar Miner

List of variants reported as likely pathogenic for Epilepsy

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Total variants: 3
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HGVS dbSNP
NM_006186.4(NR4A2):c.327dup (p.Ser110fs) rs1553456695
NM_014191.4(SCN8A):c.4423G>A (p.Gly1475Arg) rs796053216
NM_020361.5(CPA6):c.931C>T (p.Arg311Ter) rs139145929

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