RS786200960 KAT6A

Health Risk Chr 8:41934835
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
Inborn genetic diseases
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
Inborn genetic diseases
Other Variants in KAT6A
rs786200956 rs786200959 rs786200961 rs786200952 rs139494583 rs374290942 rs886041825 rs886041480 rs886042000 rs886041731
Ask Dr. Hemsworth about this variant