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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANK2, LOC126807137
(R2416Q +4 more)
Single nucleotide variant
(missense variant +1 more)
Long QT syndrome
+4 more
GUncertain significance
ANK2, LOC126807137
(R2466H +4 more)
Single nucleotide variant
(missense variant +1 more)
Cardiac arrhythmia, ankyrin-B-related
+4 more
GLikely benign
ANK2, LOC126807137
(H2486Q +4 more)
Single nucleotide variant
(missense variant +1 more)
Long QT syndrome
+2 more
GConflicting classifications of pathogenicity
LOC126807137, ANK2
(S2526L +4 more)
Single nucleotide variant
(intron variant +1 more)
Long QT syndrome
+2 more
GUncertain significance
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