RS768171831 COL1A2

Health Risk Chr 7:94426011
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What This Variant Does
"CLNSIG=4
Associated Conditions
Osteogenesis imperfecta with normal sclerae
dominant form
Osteogenesis imperfecta
perinatal lethal
Osteogenesis imperfecta type III
Ehlers-Danlos syndrome
classic type
1
Osteogenesis imperfecta type I
Cardiovascular phenotype
Osteogenesis imperfecta with normal sclerae
dominant form
Osteogenesis imperfecta
perinatal lethal
Osteogenesis imperfecta type III
Other Variants in COL1A2
rs72656357 rs72659319 rs72659345 rs74315146 rs121912900 rs121912901 rs121912902 rs121912903 rs121912904 rs121912905
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