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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RIT1
(G78E +2 more)
Single nucleotide variant
(missense variant)
Noonan syndrome 8
GConflicting classifications of pathogenicity
RIT1
(A77T +2 more)
Single nucleotide variant
(missense variant)
Noonan syndrome 8
+3 more
GPathogenic/Likely pathogenic