List of variants in gene KCNC2 reported as pathogenic for 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_139137.4(KCNC2):c.1052G>A (p.Arg351Lys)	rs2136944684
NM_139137.4(KCNC2):c.1163T>C (p.Phe388Ser)
NM_139137.4(KCNC2):c.1309A>G (p.Thr437Ala)	rs2136943757
NM_139137.4(KCNC2):c.1411G>C (p.Val471Leu)	rs2136943353
NM_139137.4(KCNC2):c.375C>G (p.Cys125Trp)	rs61735712
NM_139137.4(KCNC2):c.404A>G (p.Glu135Gly)	rs2137828445
NM_139137.4(KCNC2):c.499G>T (p.Asp167Tyr)	rs2137827783

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