List of variants in gene SLC32A1 reported as pathogenic for generalized epilepsy

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_080552.3(SLC32A1):c.1382G>A (p.Gly461Asp)	rs2084286884
NM_080552.3(SLC32A1):c.1391C>G (p.Thr464Arg)	rs2084286911
NM_080552.3(SLC32A1):c.1403T>C (p.Leu468Pro)	rs2084286998
NM_080552.3(SLC32A1):c.989T>C (p.Met330Thr)	rs2084284179

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