RS121912951 COL11A2

Health Risk Chr 6:33167822
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Otospondylomegaepiphyseal dysplasia
autosomal recessive
Fibrochondrogenesis 2
autosomal dominant
Autosomal dominant nonsyndromic hearing loss 13
Autosomal recessive nonsyndromic hearing loss 53
Otospondylomegaepiphyseal dysplasia
autosomal recessive
Fibrochondrogenesis 2
autosomal dominant
Autosomal dominant nonsyndromic hearing loss 13
Autosomal recessive nonsyndromic hearing loss 53
Other Variants in COL11A2
rs750995470 rs121912945 rs864309477 rs121912946 rs121912947 rs121912948 rs121912949 rs121912950 rs121912952 rs1562315748
Ask Dr. Hemsworth about this variant