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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHRNB2
(K110T)
Single nucleotide variant
(missense variant)
Seizure
+6 more
GConflicting classifications of pathogenicity
PTPN11
(E139D +1 more)
Single nucleotide variant
(missense variant)
Noonan syndrome
GPathogenic