RS398122378 MIP

Health Risk Chr 12:56451434
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What This Variant Does
"CLNSIG=5
Associated Conditions
Cataract 15 multiple types
MIP-related disorder
Inborn genetic diseases
Cataract 15 multiple types
MIP-related disorder
Inborn genetic diseases
Other Variants in MIP
rs1555179713 rs2547313222 rs2547312839 rs2547312066 rs2547312891 rs2136164671 rs1220143491 rs2547312090 rs1868687508 rs121917867
Ask Dr. Hemsworth about this variant