RS80358317 LRP5

Health Risk Chr 11:68425226
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Exudative vitreoretinopathy 4
Osteogenesis imperfecta
LRP5-related disorder
Inborn genetic diseases
6 conditions
Exudative vitreoretinopathy 4
Osteogenesis imperfecta
LRP5-related disorder
Inborn genetic diseases
6 conditions
Other Variants in LRP5
rs121908660 rs121908661 rs1554967141 rs121908662 rs121908663 rs80358319 rs121908664 rs121908665 rs4988321 rs121908666
Ask Dr. Hemsworth about this variant