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

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000814.6(GABRB3):c.146A>G (p.Asp49Gly)	rs2140199587
NM_000814.6(GABRB3):c.695G>C (p.Arg232Pro)	rs797045045
NM_000814.6(GABRB3):c.766C>G (p.Leu256Val)	rs1555401942
NM_000814.6(GABRB3):c.901C>T (p.Pro301Ser)	rs1889966666

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