RS60035576 KRT10

Health Risk Chr 17:40819590
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What This Variant Does
"CLNSIG=5
Associated Conditions
Epidermolytic hyperkeratosis 2B
autosomal recessive
Epidermolytic hyperkeratosis 2B
autosomal recessive
Other Variants in KRT10
rs60118264 rs57784225 rs58414354 rs58075662 rs58026994 rs58852768 rs58901407 rs61434181 rs59075499 rs587776815
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