RS80358322 LRP5

Health Risk Chr 11:68439918
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What This Variant Does
"[OMIM:?]
Associated Conditions
Exudative vitreoretinopathy 4
autosomal dominant
Familial exudative vitreoretinopathy
Inborn genetic diseases
Retinal dystrophy
Osteoporosis with pseudoglioma
Ovarian serous cystadenocarcinoma
Exudative vitreoretinopathy 4
autosomal dominant
Familial exudative vitreoretinopathy
Inborn genetic diseases
Retinal dystrophy
Osteoporosis with pseudoglioma
Ovarian serous cystadenocarcinoma
Other Variants in LRP5
rs121908660 rs121908661 rs1554967141 rs121908662 rs121908663 rs80358319 rs121908664 rs121908665 rs4988321 rs121908666
Ask Dr. Hemsworth about this variant