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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGD1
(N604S)
Single nucleotide variant
(missense variant)
Aarskog syndrome
+1 more
GUncertain significance
FGD1
Single nucleotide variant
(synonymous variant)
Aarskog syndrome
GUncertain significance
FGD1
(P182fs)
Deletion
(frameshift variant)
Aarskog syndrome
GPathogenic
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