RS115347245 PYGM

Health Risk Chr 11:64751405 snv missense variant

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Associated Conditions

Glycogen storage disease

type V

Inborn genetic diseases

Glycogen storage disease

type V

Inborn genetic diseases

Population Frequencies

gnomAD ALL

100%

1kG AFR

99.7%

1kG ALL

0.1%

1kG AMR

100%

1kG EAS

100%

1kG EUR

100%

1kG SAS

100%

Other Variants in PYGM