RS863225043 CRTAP

Health Risk Chr 3:33114195
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What This Variant Does
"CLNSIG=5
Associated Conditions
Osteogenesis imperfecta type 7
Osteogenesis imperfecta type 7
Other Variants in CRTAP
rs72659360 rs72659362 rs72659359 rs72659361 rs72659357 rs137853940 rs387907333 rs387907334 rs137853943 rs149119710
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