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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTPN23
(T175M +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity
+1 more
GUncertain significance
PTPN23
(S1389* +1 more)
Duplication
(nonsense)
Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity
GUncertain significance
AMT, APEH
+177 more
Copy number gain
not provided
GPathogenic
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