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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDE11A
(I515T +3 more)
Single nucleotide variant
(missense variant)
Pigmented nodular adrenocortical disease, primary, 2
GUncertain significance
PDE11A
(R79* +1 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GConflicting classifications of pathogenicity
PDE11A
(P165T)
Single nucleotide variant
(missense variant +1 more)
Pigmented nodular adrenocortical disease, primary, 2
GUncertain significance
DSC2
(R375*)
Single nucleotide variant
(nonsense)
Pigmented nodular adrenocortical disease, primary, 2
+2 more
GConflicting classifications of pathogenicity
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