rs11556924, ZC3HC1

N. diseases: 21
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 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.840 0.875 8 2013 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.810 1.000 5 2011 2017
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 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
281 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.030 1.000 3 2013 2019
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 2 2016 2017
Age at menarche
CUI: C1314691
Disease: Age at menarche
591 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2019 2019
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2016 2016
Body Height
CUI: C0005890
Disease: Body Height
3972 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2019 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2019 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2014 2014
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
CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
35 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2013 2013
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 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
1085 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
704 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.010 1.000 1 2019 2019
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2015 2015
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2016 2016
RDW - Red blood cell distribution width result
988 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2019 2019
Red cell distribution width determination
988 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2019 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.010 1.000 1 2013 2013
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2016 2016