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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RIT1
Single nucleotide variant
(intron variant)
Noonan syndrome 8
+2 more
GBenign
RIT1
Single nucleotide variant
(synonymous variant)
not provided
+4 more
GBenign
RIT1
(G95A +2 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+6 more
GPathogenic
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