RS58852768 KRT10

Health Risk Chr 17:40822120
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital reticular ichthyosiform erythroderma
Annular epidermolytic ichthyosis
Epidermolytic ichthyosis
Epidermolytic acanthoma
KRT10-related disorder
Epidermolytic nevus
Epidermolytic hyperkeratosis 2A
autosomal dominant
Autosomal dominant epidermolytic ichthyosis
Congenital reticular ichthyosiform erythroderma
Annular epidermolytic ichthyosis
Epidermolytic ichthyosis
Epidermolytic acanthoma
KRT10-related disorder
Epidermolytic nevus
Other Variants in KRT10
rs60118264 rs57784225 rs58414354 rs58075662 rs58026994 rs58901407 rs61434181 rs59075499 rs587776815 rs587776816
Ask Dr. Hemsworth about this variant