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.
Geographic Atrophy
CUI: C1536085
Disease: Geographic Atrophy
81 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.010 1.000 1 2016 2016
Disseminated Intravascular Coagulation
CUI: C0012739
Disease: Disseminated Intravascular Coagulation
3 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.010 1.000 1 2017 2017
exudative macular degeneration
CUI: C2237660
Disease: exudative macular degeneration
69 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.700 1.000 1 2017 2017
Lupus Nephritis
CUI: C0024143
Disease: Lupus Nephritis
64 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.010 1.000 1 2017 2017
Matrix Metalloproteinase 8 Measurement
CUI: C2698027
Disease: Matrix Metalloproteinase 8 Measurement
2 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.700 1.000 1 2017 2017
Thrombotic Microangiopathies
CUI: C2717961
Disease: Thrombotic Microangiopathies
8 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.010 1.000 1 2017 2017
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.010 1.000 1 2018 2018
Acute central serous chorioretinopathy
CUI: C0730315
Disease: Acute central serous chorioretinopathy
3 0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 0.010 1.000 1 2019 2019