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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANK2
(G47W +5 more)
Single nucleotide variant
(missense variant)
Long QT syndrome
+1 more
GUncertain significance
ANK2
(A174V +5 more)
Single nucleotide variant
(missense variant)
Long QT syndrome
+2 more
GUncertain significance
ANK2
(V1167L +37 more)
Single nucleotide variant
(missense variant +1 more)
Long QT syndrome
+3 more
GConflicting classifications of pathogenicity
ANK2, LOC126807137
(R2466C +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
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