RS112292549 TGM5

Health Risk Chr 15:43260150 snv missense variant

Upload your DNA to see your genotype for this variant.

What This Variant Does

"[OMIM:?]

Associated Conditions

Acral peeling skin syndrome

Inborn genetic diseases

TGM5-related disorder

Acral peeling skin syndrome

Inborn genetic diseases

TGM5-related disorder

Population Frequencies

gnomAD ALL

0.3%

1kG AFR

100%

1kG ALL

99.9%

1kG AMR

99.9%

1kG EAS

100%

1kG EUR

0.2%

1kG SAS

99.6%

Other Variants in TGM5