RS117208167 COG1

Health Risk Chr 17:73197385 snv missense variant

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Associated Conditions

COG1 congenital disorder of glycosylation

COG1-related disorder

COG1 congenital disorder of glycosylation

COG1-related disorder

Population Frequencies

gnomAD ALL

99.2%

1kG AFR

0.1%

1kG ALL

0.3%

1kG AMR

100%

1kG EAS

99.7%

1kG EUR

99%

1kG SAS

0.3%

Other Variants in COG1