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.
Dry age-related macular degeneration
1 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2013 2013
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
exudative macular degeneration
CUI: C2237660
Disease: exudative macular degeneration
69 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.700 1.000 1 2012 2012
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
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
Glomerulonephritis, Membranoproliferative
3 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2012 2012
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
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
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.020 0.500 2 2008 2012
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
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
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
Lobular Neoplasia
CUI: C0861352
Disease: Lobular Neoplasia
3 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2012 2012
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
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2011 2011
Lupus Nephritis
CUI: C0024143
Disease: Lupus Nephritis
64 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2017 2017
Macular degeneration
CUI: C0024437
Disease: Macular degeneration
16 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.020 0.500 2 2008 2019
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
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2016 2016
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2012 2012
Membranoproliferative Glomerulonephritis, Type II
3 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2012 2012
Multifocal choroiditis
CUI: C1533060
Disease: Multifocal choroiditis
1 0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 0.010 1.000 1 2013 2013
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
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
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