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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CC2D1A
(A154T)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 3
+1 more
GUncertain significance
CC2D1A
(K528N)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 3
GUncertain significance