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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AKT1
(M458T)
Single nucleotide variant
(missense variant)
Cowden syndrome 6
GUncertain significance
AKT1
(I75M)
Single nucleotide variant
(missense variant)
Cowden syndrome 6
GUncertain significance
AKT1
(D46E)
Single nucleotide variant
(missense variant)
Cowden syndrome 6
+2 more
GConflicting classifications of pathogenicity
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