RS140077535 GFM2

Health Risk Chr 5:74726124 snv missense variant

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Associated Conditions

Combined oxidative phosphorylation deficiency 39

Inborn genetic diseases

Combined oxidative phosphorylation deficiency 39

Inborn genetic diseases

Population Frequencies

gnomAD ALL

100%

1kG AFR

0.3%

1kG ALL

99.9%

1kG AMR

100%

1kG EAS

100%

1kG EUR

100%

1kG SAS

100%

Other Variants in GFM2