rs17228212, SMAD3

N. diseases: 8
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.807 0.160 15 67166301 intron variant T/C snv 0.21 0.810 1.000 3 2007 2012
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.807 0.160 15 67166301 intron variant T/C snv 0.21 0.010 1 2013 2013
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.807 0.160 15 67166301 intron variant T/C snv 0.21 0.010 1 2013 2013
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.807 0.160 15 67166301 intron variant T/C snv 0.21 0.010 1 2013 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.807 0.160 15 67166301 intron variant T/C snv 0.21 0.010 1.000 1 2014 2014
Heart Failure, Systolic
CUI: C1135191
Disease: Heart Failure, Systolic
6 0.807 0.160 15 67166301 intron variant T/C snv 0.21 0.010 1.000 1 2014 2014
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.807 0.160 15 67166301 intron variant T/C snv 0.21 0.010 1.000 1 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.807 0.160 15 67166301 intron variant T/C snv 0.21 0.010 1 2013 2013