Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.900 0.929 10 2009 2019
dbSNP: rs7193343
rs7193343
ZFHX3
0.882 0.120 16 72995261 intron variant T/A;C snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.870 0.857 7 2009 2019
dbSNP: rs7193343
rs7193343
ZFHX3
0.882 0.120 16 72995261 intron variant T/A;C snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.710 1.000 1 2014 2016
dbSNP: rs12932445
rs12932445
ZFHX3
0.925 0.080 16 73035989 intron variant T/C snv 0.18
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.010 1.000 1 2017 2017
dbSNP: rs1381855646
rs1381855646
ZFHX3
0.925 0.080 16 72959537 synonymous variant G/A snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 < 0.001 1 2008 2008
dbSNP: rs1381855646
rs1381855646
ZFHX3
0.925 0.080 16 72959537 synonymous variant G/A snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 < 0.001 1 2008 2008
dbSNP: rs16971436
rs16971436
ZFHX3
0.851 0.080 16 72958864 missense variant T/C;G snv 1.2E-05; 7.1E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.010 1.000 1 2014 2014
dbSNP: rs16971436
rs16971436
ZFHX3
0.851 0.080 16 72958864 missense variant T/C;G snv 1.2E-05; 7.1E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2014 2014
dbSNP: rs16971436
rs16971436
ZFHX3
0.851 0.080 16 72958864 missense variant T/C;G snv 1.2E-05; 7.1E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2014 2014
dbSNP: rs16971436
rs16971436
ZFHX3
0.851 0.080 16 72958864 missense variant T/C;G snv 1.2E-05; 7.1E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2014 2014
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		0.010 1.000 1 2017 2017
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation 		0.010 1.000 1 2018 2018
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2011 2011
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.010 1.000 1 2014 2014
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2014 2014
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2016 2016
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		0.010 1.000 1 2016 2016
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.010 1.000 1 2011 2011
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs2106261
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		0.010 1.000 1 2014 2014
dbSNP: rs6499600
rs6499600
ZFHX3
1.000 0.080 16 72945475 intron variant C/T snv 0.51
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.010 1.000 1 2014 2014
dbSNP: rs879324
rs879324
ZFHX3
1.000 0.080 16 73034779 intron variant G/A snv 0.17
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.010 < 0.001 1 2020 2020