RS200151492 WNT1

Health Risk Chr 12:48981281
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Associated Conditions
Osteogenesis imperfecta
Inborn genetic diseases
Osteogenesis imperfecta
Inborn genetic diseases
Other Variants in WNT1
rs387907353 rs387907354 rs387907355 rs387907356 rs387907357 rs387907358 rs387907359 rs397514702 rs727505392 rs1555178899
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