List of variants in gene GABBR2 reported as likely benign 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_005458.8(GABBR2):c.68T>C (p.Leu23Pro)	rs933385444	0.00012
NM_005458.8(GABBR2):c.1000-3C>T
NM_005458.8(GABBR2):c.1684G>A (p.Val562Met)

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