"Blueprint Genetics"[submitter] AND "KCNE1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 13479	NM_000219.6(KCNE1):c.253G>A (p.Asp85Asn)	KCNE1 (D85N)	Single nucleotide variant (missense variant)	Long QT syndrome 5 +7 more	GConflicting classifications of pathogenicity; other; risk factor
Select item 132677	NM_000219.6(KCNE1):c.29C>T (p.Thr10Met)	KCNE1 (T10M)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity

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