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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RUSC2
(L609F)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal recessive 61
GUncertain significance
RUSC2
Single nucleotide variant
(splice donor variant)
Intellectual disability, autosomal recessive 61
GPathogenic