RS797044854 ZMYND11

Health Risk Chr 10:252459
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Intellectual disability
autosomal dominant 30
Global developmental delay
Neurodevelopmental disorder
ZMYND11-related disorder
Inborn genetic diseases
Intellectual disability
autosomal dominant 30
Global developmental delay
Neurodevelopmental disorder
ZMYND11-related disorder
Other Variants in ZMYND11
rs606231266 rs606231267 rs672601340 rs606231268 rs672601341 rs869320713 rs1057518219 rs1057518121 rs1060499626 rs1135401771
Ask Dr. Hemsworth about this variant