ClinVar Miner

List of variants reported as likely pathogenic for Epilepsy, childhood absence 5

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Total variants: 2
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NM_000814.6(GABRB3):c.695G>C (p.Arg232Pro) rs797045045
NM_000814.6(GABRB3):c.766C>G (p.Leu256Val) rs1555401942

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