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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CRADD
Single nucleotide variant
(intron variant)
Intellectual disability, autosomal recessive 34
GUncertain significance
CRADD
Single nucleotide variant
(5 prime UTR variant +1 more)
Intellectual disability, autosomal recessive 34
GUncertain significance
CRADD
(I106F)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal recessive 34
GUncertain significance
CRADD
(R166H)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal recessive 34
+2 more
GUncertain significance
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