rs2106261, ZFHX3

N. diseases: 11
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.
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.763 0.160 16 73017721 intron variant C/G;T snv 0.900 0.929 14 2009 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2011 2011
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2011 2011
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2014 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2014 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2014 2014
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2016 2016
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2016 2016
Cerebral Infarction
CUI: C0007785
Disease: Cerebral Infarction
123 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2017 2017
Cholangiocarcinoma
CUI: C0206698
Disease: Cholangiocarcinoma
43 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2018 2018
Paroxysmal atrial fibrillation
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
8 0.763 0.160 16 73017721 intron variant C/G;T snv 0.010 1.000 1 2018 2018