Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800775
rs1800775
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.710 1.000 2 2013 2018
dbSNP: rs5882
rs5882
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.060 1.000 6 2009 2019
dbSNP: rs708272
rs708272
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.060 0.833 6 2013 2018
dbSNP: rs1800777
rs1800777
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.020 1.000 2 2012 2014
dbSNP: rs1532624
rs1532624
0.851 0.160 16 56971567 intron variant C/A snv 0.34
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs1801706
rs1801706
1.000 0.040 16 56983750 3 prime UTR variant G/A snv 0.17
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2303790
rs2303790
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2002 2002
dbSNP: rs5880
rs5880
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs5883
rs5883
1.000 0.040 16 56973441 synonymous variant C/T snv 5.1E-02 6.6E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2012 2012