RS886039477 ANKRD11

Health Risk Chr 16:89282771
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
KBG syndrome
Rare genetic intellectual disability
Inborn genetic diseases
KBG syndrome
Rare genetic intellectual disability
Other Variants in ANKRD11
rs863223319 rs863223320 rs863223321 rs797044900 rs797044890 rs797045027 rs863225257 rs201522384 rs869312713 rs878855327
Ask Dr. Hemsworth about this variant