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
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
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
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
Nevus elasticus
CUI: C0473583
Disease: Nevus elasticus
5 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2008 2008
Pseudoxanthoma Elasticum
CUI: C0033847
Disease: Pseudoxanthoma Elasticum
323 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1 2008 2008
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
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2009 2009
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2009 2009
Hypercholesterolemia, Familial
CUI: C0020445
Disease: Hypercholesterolemia, Familial
1423 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2009 2009
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2009 2009
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
56 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2009 2009
Disorder of eye
CUI: C0015397
Disease: Disorder of eye
14 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2010 2010
Systemic Inflammatory Response Syndrome
CUI: C0242966
Disease: Systemic Inflammatory Response Syndrome
9 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2010 2010
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
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
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
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2011 2011