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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLCN4
(D44N)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, X-linked 49
GUncertain significance
CLCN4
(R297S +1 more)
Single nucleotide variant
(missense variant)
Rare genetic intellectual disability
GUncertain significance