RS2534685364 COL11A2

Health Risk Chr 6:33168980
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 53
Autosomal dominant nonsyndromic hearing loss 13
Fibrochondrogenesis 2
Otospondylomegaepiphyseal dysplasia
autosomal dominant
autosomal recessive
Autosomal recessive nonsyndromic hearing loss 53
Autosomal dominant nonsyndromic hearing loss 13
Fibrochondrogenesis 2
Otospondylomegaepiphyseal dysplasia
autosomal dominant
autosomal recessive
Other Variants in COL11A2
rs750995470 rs121912945 rs864309477 rs121912946 rs121912947 rs121912948 rs121912949 rs121912950 rs121912951 rs121912952
Ask Dr. Hemsworth about this variant