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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RIT1
(G95A +2 more)
Single nucleotide variant
(missense variant)
Noonan syndrome
+5 more
GPathogenic
RIT1
(F82L +2 more)
Single nucleotide variant
(missense variant)
Noonan syndrome and Noonan-related syndrome
+7 more
GPathogenic/Likely pathogenic
RIT1
(A57G +2 more)
Single nucleotide variant
(missense variant)
RASopathy
+7 more
GPathogenic
RIT1
(S35T +1 more)
Single nucleotide variant
(missense variant +1 more)
RASopathy
+3 more
GPathogenic
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