RS116378993 FRAS1

Health Risk Chr 4:78379946 snv missense variant

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Associated Conditions

Fraser syndrome 1

Inborn genetic diseases

FRAS1-related disorder

Fraser syndrome 1

Inborn genetic diseases

FRAS1-related disorder

Population Frequencies

gnomAD ALL

100%

1kG AFR

0.6%

1kG ALL

0.2%

1kG AMR

100%

1kG EAS

100%

1kG EUR

100%

1kG SAS

100%

Other Variants in FRAS1