RS67815019 COL1A1

Health Risk Chr 17:50187041
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What This Variant Does
"CLNSIG=5
Associated Conditions
Osteogenesis imperfecta type I
Osteogenesis imperfecta
Abnormality of the skeletal system
Infantile cortical hyperostosis
Osteogenesis imperfecta type I
Osteogenesis imperfecta
Abnormality of the skeletal system
Infantile cortical hyperostosis
Other Variants in COL1A1
rs72645333 rs72645331 rs66721653 rs72648363 rs67368147 rs72651651 rs72653137 rs72653136 rs72653143 rs72653152
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