rs800292, CFH

N. diseases: 33
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Nephritis
CUI: C0027697
Disease: Nephritis
40 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.010 1.000 1 2011 2011
Retinal Pigment Epithelial Detachment
3 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.010 1 2011 2011
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.010 1 2011 2011
Retinal angiomatous proliferation
CUI: C2609315
Disease: Retinal angiomatous proliferation
4 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.020 1.000 2 2010 2017
Polypoidal choroidal vasculopathy
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
67 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.100 1.000 12 2008 2017
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
269 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.100 1.000 10 2008 2018
Membranoproliferative Glomerulonephritis, Type II
3 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.020 1.000 2 2008 2011
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.900 0.980 51 2005 2019