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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRADD
(M1R)
Single nucleotide variant
(missense variant +2 more)
Intellectual disability, moderate
GPathogenic
USP44
(L291fs)
Indel
(frameshift variant +1 more)
Intellectual disability, moderate
GUncertain significance