RS72659351 P3H1

Health Risk Chr 1:42757782
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What This Variant Does
"CLNSIG=5
Associated Conditions
Osteogenesis imperfecta type 8
Osteogenesis imperfecta
P3H1-related disorder
Osteogenesis imperfecta type III
Osteogenesis imperfecta type 8
Osteogenesis imperfecta
P3H1-related disorder
Osteogenesis imperfecta type III
Other Variants in P3H1
rs72659354 rs72659348 rs72659355 rs137853952 rs118203996 rs137853890 rs786205443 rs533729683 rs770943260 rs765846480
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