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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGD1
(D529E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FGD1
(P200S)
Single nucleotide variant
(missense variant)
Aarskog syndrome
GUncertain significance