RS61371557 KRT14
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What This Variant Does
"[OMIM:?]
Associated Conditions
Epidermolysis bullosa simplex
Koebner type
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex 1D
generalized
intermediate or severe
autosomal recessive
Epidermolysis bullosa simplex 1A
generalized severe
Epidermolysis bullosa simplex
Koebner type
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex 1D
generalized
intermediate or severe
Other Variants in KRT14