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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGD1, TSR2
(R958Q)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
FGD1, TSR2
(R935G)
Single nucleotide variant
(missense variant +1 more)
Aarskog syndrome
GUncertain significance
FGD1, TSR2
(Y854C)
Single nucleotide variant
(missense variant +1 more)
Aarskog syndrome
GUncertain significance
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