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.
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
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
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
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
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
Reticular pseudodrusen
CUI: C2609282
Disease: Reticular pseudodrusen
10 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.040 1.000 4 2016 2019
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
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.030 1.000 3 2008 2016
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.030 1.000 3 2008 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.030 1.000 3 2008 2012
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
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.020 1.000 2 2010 2015
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.020 1.000 2 2010 2020
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.020 1.000 2 2010 2020
Acute central serous chorioretinopathy
3 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2019 2019
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
Bacterial Infections
CUI: C0004623
Disease: Bacterial Infections
17 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2020 2020
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.700 1.000 1 2018 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2012 2012
Chronic Fatigue Syndrome
CUI: C0015674
Disease: Chronic Fatigue Syndrome
14 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2015 2015
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
2672 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