RS886041303 CAPN5

Health Risk Chr 11:77115560
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What This Variant Does
"CLNSIG=5
Associated Conditions
Proliferative vitreoretinopathy
Inborn genetic diseases
CAPN5-related disorder
Proliferative vitreoretinopathy
Inborn genetic diseases
CAPN5-related disorder
Other Variants in CAPN5
rs782717683 rs149759840 rs374146255 rs538890890 rs782125333 rs534203457 rs372227864 rs374843302 rs199893083 rs397514601
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