RS80358312 LRP5

Health Risk Chr 11:68403607
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What This Variant Does
"[OMIM:?]
Associated Conditions
Exudative vitreoretinopathy 4
autosomal recessive
Inborn genetic diseases
Retinal dystrophy
Exudative vitreoretinopathy 4
autosomal recessive
Inborn genetic diseases
Retinal dystrophy
Other Variants in LRP5
rs121908660 rs121908661 rs1554967141 rs121908662 rs121908663 rs80358319 rs121908664 rs121908665 rs4988321 rs121908666
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