RS3219484 MUTYH

Health Risk Chr 1:45334483 snv missense variant

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Associated Conditions

Hereditary cancer-predisposing syndrome

Familial adenomatous polyposis 2

Hereditary cancer-predisposing syndrome

Familial adenomatous polyposis 2

Population Frequencies

gnomAD ALL

6.5%

1kG AFR

0.2%

1kG ALL

98%

1kG AMR

97.7%

1kG EAS

0.2%

1kG EUR

94.6%

1kG SAS

97.1%

Other Variants in MUTYH