RS72659325 COL1A2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Osteogenesis imperfecta with normal sclerae
dominant form
Short fetal femur length
See cases
Osteogenesis imperfecta type I
Ehlers-Danlos syndrome
classic type
1
Osteogenesis imperfecta type I
Ehlers-Danlos syndrome
classic type
1
Osteogenesis imperfecta with normal sclerae
dominant form
Short fetal femur length
Other Variants in COL1A2