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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNE1
(D85N)
Single nucleotide variant
(missense variant)
Long QT syndrome 5
+7 more
GConflicting classifications of pathogenicity; other; risk factor
KCNE1
(S38G)
Single nucleotide variant
(missense variant)
Congenital long QT syndrome
+7 more
GBenign
KCNE1
(S37G)
Indel
(missense variant)
Cardiovascular phenotype
+4 more
GUncertain significance
KCNE1
Single nucleotide variant
(synonymous variant)
Long QT syndrome 5
+5 more
GBenign/Likely benign
KCNE1
Single nucleotide variant
(synonymous variant)
Jervell and Lange-Nielsen syndrome 2
+6 more
GBenign/Likely benign
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