rs56062135, 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 Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.790 0.200 15 67163292 intron variant C/T snv 0.18 0.710 1.000 3 2015 2018
Adult onset asthma
CUI: C0741260
Disease: Adult onset asthma
67 0.790 0.200 15 67163292 intron variant C/T snv 0.18 0.700 1.000 1 2019 2019
Allergic Reaction
CUI: C1527304
Disease: Allergic Reaction
1019 0.790 0.200 15 67163292 intron variant C/T snv 0.18 0.700 1.000 1 2018 2018
Asthma
CUI: C0004096
Disease: Asthma
1536 0.790 0.200 15 67163292 intron variant C/T snv 0.18 0.700 1.000 1 2018 2018
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.790 0.200 15 67163292 intron variant C/T snv 0.18 0.700 1.000 1 2019 2019
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.790 0.200 15 67163292 intron variant C/T snv 0.18 0.700 1.000 1 2017 2017
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.790 0.200 15 67163292 intron variant C/T snv 0.18 0.010 1.000 1 2016 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.790 0.200 15 67163292 intron variant C/T snv 0.18 0.010 1.000 1 2016 2016