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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RIT1
(V138I +2 more)
Single nucleotide variant
(missense variant)
Noonan syndrome 8
GUncertain significance
RIT1
(F82V +2 more)
Single nucleotide variant
(missense variant)
Noonan syndrome and Noonan-related syndrome
+4 more
GPathogenic