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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNJ2
(C154Y)
Single nucleotide variant
(missense variant)
Andersen Tawil syndrome
+1 more
GConflicting classifications of pathogenicity
KCNJ2
(R218Q)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic
KCNJ2
Single nucleotide variant
(synonymous variant)
not provided
+5 more
GBenign
KCNJ2
(T402M)
Single nucleotide variant
(missense variant)
not specified
+3 more
GUncertain significance
KCNJ2
(N410S)
Single nucleotide variant
(missense variant)
Andersen Tawil syndrome
+5 more
GConflicting classifications of pathogenicity
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