RS146555195 COL11A2

Health Risk Chr 6:33164337
Upload your DNA to see your genotype for this variant.
Associated Conditions
Fibrochondrogenesis 2
Otospondylomegaepiphyseal dysplasia
autosomal recessive
Connective tissue disorder
Autosomal recessive nonsyndromic hearing loss 53
Fibrochondrogenesis 2
Otospondylomegaepiphyseal dysplasia
autosomal recessive
Connective tissue disorder
Autosomal recessive nonsyndromic hearing loss 53
Other Variants in COL11A2
rs750995470 rs121912945 rs864309477 rs121912946 rs121912947 rs121912948 rs121912949 rs121912950 rs121912951 rs121912952
Ask Dr. Hemsworth about this variant