RS60399023 KRT14
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What This Variant Does
"[OMIM:?]
Associated Conditions
Epidermolysis bullosa simplex 1A
generalized severe
Epidermolysis bullosa simplex
Koebner type
KRT14-related disorder
Inborn genetic diseases
Epidermolysis bullosa simplex 1A
generalized severe
Epidermolysis bullosa simplex
Koebner type
KRT14-related disorder
Inborn genetic diseases
Other Variants in KRT14