RS386834093 VPS13B

Health Risk Chr 8:99575719
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Cohen syndrome
Inborn genetic diseases
VPS13B-related disorder
Cohen syndrome
Inborn genetic diseases
VPS13B-related disorder
Other Variants in VPS13B
rs180177327 rs120074149 rs120074150 rs28940272 rs120074151 rs120074152 rs120074153 rs120074154 rs180177329 rs386834054
Ask Dr. Hemsworth about this variant