rs17611, C5

N. diseases: 14
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.
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.020 1.000 2 2012 2016
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.020 1.000 2 2016 2016
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2012 2012
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2012 2012
Carotid Atherosclerosis
CUI: C0577631
Disease: Carotid Atherosclerosis
79 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2012 2012
Carotid Stenosis
CUI: C0007282
Disease: Carotid Stenosis
19 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2012 2012
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2016 2016
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2019 2019
Meningitis, Bacterial
CUI: C0085437
Disease: Meningitis, Bacterial
16 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2011 2011
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2009 2009
Neurocysticercosis
CUI: C0338437
Disease: Neurocysticercosis
9 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2019 2019
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2010 2010
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 0.010 1.000 1 2015 2015