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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SOS2
(N921S +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
SOS2
(V847G)
Single nucleotide variant
(missense variant)
Noonan syndrome 9
GUncertain significance