RS199866657 COL11A2

Health Risk Chr 6:33178948
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Associated Conditions
Otospondylomegaepiphyseal dysplasia
autosomal recessive
Fibrochondrogenesis 2
autosomal dominant
Inborn genetic diseases
Hearing impairment
COL11A2-related disorder
Otospondylomegaepiphyseal dysplasia
autosomal recessive
Fibrochondrogenesis 2
autosomal dominant
Inborn genetic diseases
Hearing impairment
COL11A2-related disorder
Other Variants in COL11A2
rs750995470 rs121912945 rs864309477 rs121912946 rs121912947 rs121912948 rs121912949 rs121912950 rs121912951 rs121912952
Ask Dr. Hemsworth about this variant