List of variants in gene KCNT2 reported as likely 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_198503.5(KCNT2):c.1096A>G (p.Lys366Glu)	rs2148529666
NM_198503.5(KCNT2):c.1667C>T (p.Thr556Ile)
NM_198503.5(KCNT2):c.1731_1738del (p.Phe578fs)	rs2148151806
NM_198503.5(KCNT2):c.2501_2507del (p.Ser834fs)	rs2147978696
NM_198503.5(KCNT2):c.3055C>T (p.Arg1019Ter)
NM_198503.5(KCNT2):c.433del (p.Ile145fs)
NM_198503.5(KCNT2):c.800T>A (p.Leu267His)
NM_198503.5(KCNT2):c.914G>C (p.Cys305Ser)	rs2148537524

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