"Women's Health and Genetics/Laboratory Corporation of America, LabCor - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 137990	NM_000890.5(KCNJ5):c.171T>C (p.Ser57=)	KCNJ5	Single nucleotide variant (synonymous variant)	Congenital long QT syndrome +5 more	GBenign
Select item 432222	NM_000890.5(KCNJ5):c.439G>A (p.Glu147Lys)	KCNJ5 (E147K)	Single nucleotide variant (missense variant)	Long QT syndrome 13 +5 more	GUncertain significance
Select item 1443642	NM_000890.5(KCNJ5):c.590C>T (p.Ala197Val)	KCNJ5 (A197V)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 137991	NM_000890.5(KCNJ5):c.810T>G (p.Leu270=)	KCNJ5	Single nucleotide variant (synonymous variant)	Congenital long QT syndrome +5 more	GBenign
Select item 137992	NM_000890.5(KCNJ5):c.834T>C (p.His278=)	KCNJ5	Single nucleotide variant (synonymous variant)	Congenital long QT syndrome +5 more	GBenign
Select item 137993	NM_000890.5(KCNJ5):c.844C>G (p.Gln282Glu)	KCNJ5 (Q282E)	Single nucleotide variant (missense variant)	KCNJ5-related condition +6 more	GBenign
Select item 137994	NM_000890.5(KCNJ5):c.937+7C>T	KCNJ5	Single nucleotide variant (intron variant)	Congenital long QT syndrome +3 more	GBenign
Select item 137995	NM_000890.5(KCNJ5):c.938-10G>A	KCNJ5	Single nucleotide variant (intron variant)	Congenital long QT syndrome +4 more	GBenign

ClinVar