List of variants in gene GABBR2 reported as pathogenic for epilepsy

Minimum submission review status:		Collection method:
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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.2077G>T (p.Gly693Trp)	rs1554689320
NM_005458.8(GABBR2):c.2084G>T (p.Ser695Ile)	rs1554689319
NM_005458.8(GABBR2):c.2114T>A (p.Ile705Asn)	rs1554689315

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