ClinVar Miner

List of variants studied for Epilepsy, childhood absence, susceptibility to, 5 by OMIM

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_021912.5(GABRB3):c.31C>T (p.Pro11Ser) rs25409 0.00354
NM_021912.5(GABRB3):c.44C>T (p.Ser15Phe) rs121913126 0.00016
NM_000814.6(GABRB3):c.94G>A (p.Gly32Arg) rs71651682

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