rs11556924, ZC3HC1

N. diseases: 9
Source: BEFREE ×
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
1022 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.840 0.875 4 2013 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
769 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.810 1.000 1 2011 2017
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
266 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.030 1.000 3 2013 2019
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
271 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.030 1.000 3 2013 2019
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.010 1.000 1 2017 2017
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
291 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.010 1.000 1 2015 2015
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
871 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.010 1.000 1 2015 2015
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
586 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.010 1.000 1 2019 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.010 1.000 1 2013 2013