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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CNKSR2
(R428* +1 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
CNKSR2
Single nucleotide variant
(splice donor variant)
X-linked recessive seizure and neurodevelopmental deficit
GLikely pathogenic