RS67707918 COL1A2

Health Risk Chr 7:94410501
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What This Variant Does
"CLNSIG=5
Associated Conditions
Osteogenesis imperfecta with normal sclerae
dominant form
Dentinogenesis imperfecta
Osteogenesis imperfecta
Osteogenesis imperfecta type I
Ehlers-Danlos syndrome
classic type
1
COL1A2-related disorder
Osteogenesis imperfecta type I
Ehlers-Danlos syndrome
classic type
1
Osteogenesis imperfecta with normal sclerae
dominant form
Other Variants in COL1A2
rs72656357 rs72659319 rs72659345 rs74315146 rs121912900 rs121912901 rs121912902 rs121912903 rs121912904 rs121912905
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