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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHX15
(K443E)
Single nucleotide variant
(missense variant)
Seizure
+7 more
GUncertain significance
PTPN11
(Y62D +1 more)
Single nucleotide variant
(missense variant)
RASopathy
GPathogenic