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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAC1
(D57A)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 48
GUncertain significance
RAC1
(R113C +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 48
GUncertain significance
RAC1
(L160V +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 48
GUncertain significance
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