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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SOS1
(G434R +1 more)
Single nucleotide variant
(missense variant)
Noonan syndrome and Noonan-related syndrome
+12 more
GPathogenic/Likely pathogenic
HRAS, LRRC56
(I93V)
Single nucleotide variant
(missense variant +1 more)
RASopathy
GUncertain significance