rs1061170, CFH

N. diseases: 72
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.
MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
CUI: C1853147
Disease: MACULAR DEGENERATION, AGE-RELATED, 4 (disorder)
5 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.700 0
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.900 0.936 218 2005 2019
Exudative age-related macular degeneration
CUI: C0271084
Disease: Exudative age-related macular degeneration
109 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.800 0.950 20 2005 2018
Blindness
CUI: C0456909
Disease: Blindness
34 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.050 1.000 5 2005 2011
Glycogen storage disease type II
CUI: C0017921
Disease: Glycogen storage disease type II
269 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.100 0.889 27 2006 2019
Geographic Atrophy
CUI: C1536085
Disease: Geographic Atrophy
81 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.760 1.000 7 2006 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.060 1.000 6 2006 2011
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.060 1.000 6 2006 2011
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.040 1.000 4 2006 2011
Soft drusen
CUI: C1720452
Disease: Soft drusen
5 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.040 1.000 4 2006 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.030 0.333 3 2006 2007
Atherothrombosis
CUI: C1963943
Disease: Atherothrombosis
15 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1 2006 2006
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1 2006 2006
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1 2006 2006
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1 2006 2006
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.040 1.000 4 2007 2009
BASAL LAMINAR DRUSEN (disorder)
CUI: C0730295
Disease: BASAL LAMINAR DRUSEN (disorder)
5 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.720 1.000 2 2007 2012
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.020 0.500 2 2007 2012
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.020 0.500 2 2007 2012
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1 2007 2007
Atypical Hemolytic Uremic Syndrome
CUI: C2931788
Disease: Atypical Hemolytic Uremic Syndrome
42 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2007 2007
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2007 2007
Low Vision
CUI: C0042798
Disease: Low Vision
51 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2007 2007
Polypoidal choroidal vasculopathy
CUI: C1504336
Disease: Polypoidal choroidal vasculopathy
67 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.060 0.833 6 2008 2013
Drusen
CUI: C1260959
Disease: Drusen
18 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.050 1.000 5 2008 2015