RS59115483 KRT5
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex 2C
localized
KRT5-related disorder
Epidermolysis bullosa simplex 2d
generalized
intermediate or severe
autosomal recessive
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex 2C
localized
KRT5-related disorder
Epidermolysis bullosa simplex 2d
generalized
intermediate or severe
Other Variants in KRT5