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: rs4646903
rs4646903
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.040 1.000 4 2010 2017
dbSNP: rs1048943
rs1048943
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.020 1.000 2 2014 2017
dbSNP: rs1279844744
rs1279844744
0.925 0.080 15 74720521 missense variant A/G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1368310331
rs1368310331
0.827 0.200 15 74723032 synonymous variant T/C snv 7.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs4646422
rs4646422
0.882 0.120 15 74722964 missense variant C/T snv 1.1E-02 3.4E-03
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs777119337
rs777119337
0.827 0.200 15 74723018 missense variant C/T snv 4.0E-06
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2015 2015