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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RIT1
Single nucleotide variant
(intron variant)
Noonan syndrome 8
+2 more
GBenign
RIT1
(E11Q)
Single nucleotide variant
(missense variant +2 more)
not specified
+2 more
GBenign