List of variants in gene GABRB1 reported as pathogenic for epilepsy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000812.4(GABRB1):c.737T>C (p.Phe246Ser)	rs886039817
NM_000812.4(GABRB1):c.740T>C (p.Ile247Thr)	rs1728474004
NM_000812.4(GABRB1):c.860C>T (p.Thr287Ile)	rs886039818

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