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Items: 17

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ANK2
(R255K +8 more)
Single nucleotide variant
(missense variant)
Cardiac arrhythmia, ankyrin-B-related
+3 more
GUncertain significance
ANK2
(L403F +8 more)
Single nucleotide variant
(missense variant +1 more)
Long QT syndrome
+2 more
GUncertain significance
ANK2
(T445M +11 more)
Single nucleotide variant
(missense variant)
Long QT syndrome
+3 more
GUncertain significance
ANK2
(R925C +24 more)
Single nucleotide variant
(missense variant)
Cardiac arrhythmia, ankyrin-B-related
+3 more
GConflicting classifications of pathogenicity
ANK2
(G1014R +30 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
ANK2
(G1016A +30 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
ANK2
(M1340V +38 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ANK2, LOC126807136
(T1832I +4 more)
Single nucleotide variant
(missense variant +1 more)
Long QT syndrome
+2 more
GUncertain significance
ANK2, LOC126807136
(H1948Q +4 more)
Single nucleotide variant
(missense variant +1 more)
Cardiac arrhythmia, ankyrin-B-related
+1 more
GUncertain significance
ANK2, LOC126807136
(K2076N +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+5 more
GConflicting classifications of pathogenicity
ANK2, LOC126807137
(G2293V +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK2, LOC126807137
(S2655L +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
ANK2
(D2821E +4 more)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+2 more
GConflicting classifications of pathogenicity
ANK2
(R3408Q +4 more)
Single nucleotide variant
(intron variant +1 more)
Cardiac arrhythmia, ankyrin-B-related
+2 more
GUncertain significance
ANK2
(A2221S +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ANK2
(P1730A +43 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+3 more
GConflicting classifications of pathogenicity
ANK2
(G1753R +51 more)
Inversion
(missense variant +1 more)
Long QT syndrome
+1 more
GUncertain significance
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