RS786200959 KAT6A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
Syndromic intellectual disability
Inborn genetic diseases
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
Syndromic intellectual disability
Inborn genetic diseases
Other Variants in KAT6A