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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASH1L
(H2574P +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 52
GUncertain significance
ASH1L
(S517L)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 52
GUncertain significance
ASH1L
(K341E)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 52
GUncertain significance
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