rs17293632, SMAD3

N. diseases: 12
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.800 1.000 4 2010 2017
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.800 1.000 3 2012 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.700 1.000 3 2015 2017
Allergic Reaction
CUI: C1527304
Disease: Allergic Reaction
1019 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.700 1.000 1 2013 2013
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.700 1.000 1 2016 2016
Asthma
CUI: C0004096
Disease: Asthma
1536 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.700 1.000 1 2018 2018
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.700 1.000 1 2016 2016
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.700 1.000 1 2019 2019
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.700 1.000 1 2016 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.010 1.000 1 2016 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.010 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.763 0.240 15 67150258 intron variant C/T snv 0.17 0.010 1.000 1 2016 2016