RS138437966 MCM7

Health Risk Chr 7:100102941 snv missense variant

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Associated Conditions

Hereditary spastic paraplegia 50

AP4M1-related disorder

Hereditary spastic paraplegia 50

AP4M1-related disorder

Population Frequencies

gnomAD ALL

0.1%

1kG AFR

100%

1kG ALL

99.9%

1kG AMR

0.1%

1kG EAS

100%

1kG EUR

0.2%

1kG SAS

100%

Other Variants in MCM7