RS727504458 COL11A2

Health Risk Chr 6:33165594
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Associated Conditions
Inborn genetic diseases
Otospondylomegaepiphyseal dysplasia
autosomal recessive
Autosomal dominant nonsyndromic hearing loss 13
Autosomal recessive nonsyndromic hearing loss 53
Fibrochondrogenesis 2
autosomal dominant
Inborn genetic diseases
Otospondylomegaepiphyseal dysplasia
autosomal recessive
Autosomal dominant nonsyndromic hearing loss 13
Autosomal recessive nonsyndromic hearing loss 53
Fibrochondrogenesis 2
autosomal dominant
Other Variants in COL11A2
rs750995470 rs121912945 rs864309477 rs121912946 rs121912947 rs121912948 rs121912949 rs121912950 rs121912951 rs121912952
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