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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNAS
(P338Q)
Single nucleotide variant
(missense variant +2 more)
Cushing syndrome
+7 more
GUncertain significance
GNAS
(P423H)
Single nucleotide variant
(missense variant +2 more)
McCune-Albright syndrome
+8 more
GBenign/Likely benign