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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SOS2
(R784C)
Single nucleotide variant
(missense variant)
Noonan syndrome 9
GConflicting classifications of pathogenicity
SOS2
(R623H)
Single nucleotide variant
(missense variant)
Noonan syndrome 9
GUncertain significance