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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SHOC2
(A78V)
Single nucleotide variant
(missense variant)
RASopathy
+1 more
GUncertain significance
SHOC2
(V334I +1 more)
Single nucleotide variant
(missense variant +1 more)
Noonan syndrome-like disorder with loose anagen hair 1
GUncertain significance