C0151878[trait identifier] AND "Center For Human Genetics And Laborato - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 560359	NM_000218.3(KCNQ1):c.785T>C (p.Leu262Pro)	KCNQ1 (L135P +2 more)	Single nucleotide variant (missense variant)	Long QT syndrome +1 more	GPathogenic/Likely pathogenic
Select item 972690	NM_005472.5(KCNE3):c.241C>T (p.Arg81Cys)	KCNE3 (R81C)	Single nucleotide variant (missense variant)	Prolonged QT interval +2 more	GUncertain significance
Select item 972693	NM_005472.5(KCNE3):c.65A>G (p.Asn22Ser)	KCNE3 (N22S)	Single nucleotide variant (missense variant)	Prolonged QT interval	GUncertain significance

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ClinVar