RS748440351 COL11A2
Upload your DNA to see your genotype for this variant.
Associated Conditions
Heart
malformation of
Cystic hygroma
Thickened nuchal skin fold
Short long bone
Ear malformation
Autosomal recessive nonsyndromic hearing loss 53
Deafness
Otospondylomegaepiphyseal dysplasia
autosomal dominant
autosomal recessive
Fibrochondrogenesis 2
Autosomal dominant nonsyndromic hearing loss 13
Heart
malformation of
Other Variants in COL11A2