"CSER _CC_NCGL, University of Washington"[submitter] AND "KCNE2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 67621	NM_172201.2(KCNE2):c.40G>A (p.Val14Ile)	LOC105372791, KCNE2 (V14I)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GLikely benign
Select item 67623	NM_172201.2(KCNE2):c.80G>A (p.Arg27His)	LOC105372791, KCNE2 (R27H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GConflicting classifications of pathogenicity
Select item 6053	NM_172201.2(KCNE2):c.161T>C (p.Met54Thr)	KCNE2, LOC105372791 (M54T)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity; risk factor
Select item 6054	NM_172201.2(KCNE2):c.170T>C (p.Ile57Thr)	KCNE2, LOC105372791 (I57T)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity
Select item 67614	NM_172201.2(KCNE2):c.229C>T (p.Arg77Trp)	KCNE2, LOC105372791 (R77W)	Single nucleotide variant (missense variant)	Long QT syndrome 6 +4 more	GConflicting classifications of pathogenicity
Select item 67616	NM_172201.2(KCNE2):c.230G>A (p.Arg77Gln)	KCNE2, LOC105372791 (R77Q)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GConflicting classifications of pathogenicity

ClinVar