List of variants in gene GOT2 reported as 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002080.4(GOT2):c.1037T>G (p.Val346Gly)	rs30842	0.74625
NM_002080.4(GOT2):c.816C>T (p.Cys272=)	rs1058192	0.71897
NM_002080.4(GOT2):c.228T>G (p.Val76=)	rs14221	0.71031
NM_002080.4(GOT2):c.213T>C (p.Asn71=)	rs257636	0.69895

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