RS57784225 KRT10

Health Risk Chr 17:40822126
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What This Variant Does
"[OMIM:?]
Associated Conditions
Epidermolytic hyperkeratosis 2A
autosomal dominant
Epidermolytic hyperkeratosis 2A
autosomal dominant
Other Variants in KRT10
rs60118264 rs58414354 rs58075662 rs58026994 rs58852768 rs58901407 rs61434181 rs59075499 rs587776815 rs587776816
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