Source: ALL

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: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
0.010 1.000 1 2020 2020
dbSNP: rs2266788
rs2266788
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0002965
Disease: Angina, Unstable
Angina, Unstable
0.010 1.000 1 2018 2018
dbSNP: rs2075291
rs2075291
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.020 1.000 2 2009 2018
dbSNP: rs2075291
rs2075291
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.020 1.000 2 2009 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2016 2016
dbSNP: rs11823543
rs11823543
11 116778419 3 prime UTR variant G/A snv 0.11
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs2266788
rs2266788
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.700 1.000 1 2011 2011
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 2 2018 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 1 2012 2012
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.710 1.000 2 2013 2019
dbSNP: rs2075291
rs2075291
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis
0.010 1.000 1 2009 2009
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.700 1.000 1 2016 2016
dbSNP: rs2266788
rs2266788
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma
0.010 1.000 1 2018 2018
dbSNP: rs2266788
rs2266788
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.010 1.000 1 2014 2014
dbSNP: rs2266788
rs2266788
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C0751039
Disease: Cockayne Syndrome, Type I
Cockayne Syndrome, Type I
0.010 1.000 1 2018 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.020 1.000 2 2013 2018
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.730 1.000 4 2013 2018
dbSNP: rs2075291
rs2075291
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.720 1.000 2 2017 2019
dbSNP: rs2266788
rs2266788
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.020 1.000 2 2014 2018
dbSNP: rs6589566
rs6589566
0.882 0.080 11 116781707 intron variant G/A;C;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2016 2016
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 7 2011 2018
dbSNP: rs2075291
rs2075291
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 1.000 1 2013 2013
dbSNP: rs6589566
rs6589566
0.882 0.080 11 116781707 intron variant G/A;C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs964184
rs964184
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2016 2016