RS144562769 COL11A1

Health Risk Chr 1:102946896
Upload your DNA to see your genotype for this variant.
Associated Conditions
Fibrochondrogenesis 1
Stickler syndrome type 2
Hearing loss
autosomal dominant 37
Fibrochondrogenesis 1
Stickler syndrome type 2
Hearing loss
autosomal dominant 37
Other Variants in COL11A1
rs121912943 rs121912944 rs2101038943 rs730882190 rs387906611 rs1557812993 rs398122828 rs56230601 rs398123652 rs587782990
Ask Dr. Hemsworth about this variant