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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASH1L
(R2653* +1 more)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal dominant 52
GLikely pathogenic
ASH1L
(R1852Q)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 52
GUncertain significance