RS117843968 MAN2B1

Health Risk Chr 19:12663722 snv missense variant

Upload your DNA to see your genotype for this variant.

Associated Conditions

Deficiency of alpha-mannosidase

MAN2B1-related disorder

Deficiency of alpha-mannosidase

MAN2B1-related disorder

Population Frequencies

gnomAD ALL

0.5%

1kG AFR

100%

1kG ALL

99.9%

1kG AMR

0.3%

1kG EAS

100%

1kG EUR

0.4%

1kG SAS

0.1%

Other Variants in MAN2B1