Related gene-specific medical variations for Gene (Select 23416) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3113219	NM_012284.3(KCNH3):c.472G>A (p.Ala158Thr)	KCNH3, LOC126861521 (A98T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621127	NM_012284.3(KCNH3):c.560G>A (p.Gly187Asp)	KCNH3, LOC126861521 (G127D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552983	NM_012284.3(KCNH3):c.457C>T (p.Arg153Cys)	KCNH3, LOC126861521 (R93C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406602	NM_012284.3(KCNH3):c.736G>A (p.Val246Met)	KCNH3, LOC126861521 (V246M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388689	NM_012284.3(KCNH3):c.640C>T (p.Pro214Ser)	KCNH3, LOC126861521 (P154S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286645	NM_012284.3(KCNH3):c.484G>A (p.Gly162Ser)	KCNH3, LOC126861521 (G102S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270268	NM_012284.3(KCNH3):c.535G>A (p.Gly179Arg)	KCNH3, LOC126861521 (G179R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268619	NM_012284.3(KCNH3):c.775G>A (p.Gly259Ser)	KCNH3, LOC126861521 (G199S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar