RS138930771 VPS13B

Health Risk Chr 8:99642392 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Cohen syndrome
Inborn genetic diseases
VPS13B-related disorder
Cohen syndrome
Inborn genetic diseases
VPS13B-related disorder
Population Frequencies
gnomAD ALL
100%
1kG AFR
0.1%
1kG ALL
0%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in VPS13B
rs180177327 rs120074149 rs120074150 rs28940272 rs120074151 rs120074152 rs120074153 rs120074154 rs180177329 rs386834054
Ask Dr. Hemsworth about this variant