RS57499817 KRT5
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What This Variant Does
"[OMIM:?]
Associated Conditions
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex
KRT5-related disorder
Inborn genetic diseases
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex
KRT5-related disorder
Inborn genetic diseases
Other Variants in KRT5