List of variants in gene GABRA6 reported as uncertain significance for electroclinical syndrome

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_000811.3(GABRA6):c.255G>C (p.Gln85His)	rs115069685	0.00088
NM_000811.3(GABRA6):c.371C>G (p.Ser124Cys)	rs1554115593
NM_000811.3(GABRA6):c.847A>G (p.Met283Val)	rs1554115829

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