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: rs671
rs671
0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.850 1.000 1 2010 2016
dbSNP: rs1333049
rs1333049
0.715 0.286 9 22125504 intergenic variant G/C snp 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 9 2007 2018
dbSNP: rs17465637
rs17465637
0.784 0.143 1 222650187 intron variant A/C,G,T snp 0.64; 6.4E-06 0.59
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 2 2011 2014
dbSNP: rs3798220
rs3798220
LPA
0.784 0.036 6 160540105 missense variant T/C snp 5.6E-02 2.6E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 2 2010 2013
dbSNP: rs10455872
rs10455872
LPA
0.707 0.179 6 160589086 intron variant A/G snp 4.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 1 2010 2017
dbSNP: rs501120
rs501120
0.923 0.036 10 44258419 intergenic variant T/C snp 0.23
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 3 2007 2013
dbSNP: rs6922269
rs6922269
0.821 0.036 6 150931849 intron variant G/A snp 0.33
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 2 2007 2015
dbSNP: rs4977574
rs4977574
0.769 0.179 9 22098575 intron variant A/G,T snp 0.40; 3.2E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 5 2011 2015
dbSNP: rs599839
rs599839
0.784 0.143 1 109279544 intergenic variant G/A,C snp 0.64; 6.4E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 3 2007 2014
dbSNP: rs11206510
rs11206510
0.846 0.107 1 55030366 intergenic variant T/C,G snp 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2013
dbSNP: rs1122608
rs1122608
0.784 0.071 19 11052925 intron variant G/T snp 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2014
dbSNP: rs12526453
rs12526453
0.878 0.036 6 12927312 intron variant C/G snp 0.25
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2017
dbSNP: rs2259816
rs2259816
1.000 0.036 12 120997784 synonymous variant G/A,T snp 6.7E-06; 0.40 3.2E-05; 0.31
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2009 2012
dbSNP: rs2943634
rs2943634
0.801 0.107 2 226203364 intergenic variant A/C,G snp 0.61; 5.6E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2007 2012
dbSNP: rs10757274
rs10757274
0.821 0.071 9 22096056 intron variant A/G snp 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2008 2012
dbSNP: rs646776
rs646776
0.801 0.214 1 109275908 regulatory region variant C/T snp 0.75
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 3 2011 2012
dbSNP: rs17228212
rs17228212
0.846 0.143 15 67166301 intron variant T/C snp 0.20
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 2 2007 2012
dbSNP: rs964184
rs964184
0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 2 2011 2016
dbSNP: rs12190287
rs12190287
0.821 0.071 6 133893387 3 prime UTR variant C/G,T snp 0.31; 2.1E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2014
dbSNP: rs17114036
rs17114036
0.878 0.036 1 56497149 intron variant A/G snp 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2014
dbSNP: rs174547
rs174547
0.846 0.071 11 61803311 intron variant T/C snp 0.30
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 < 0.001 1 2011 2016
dbSNP: rs3825807
rs3825807
0.801 0.036 15 78796769 missense variant A/G snp 0.34 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2014
dbSNP: rs4420638
rs4420638
0.724 0.321 19 44919689 intergenic variant A/G snp 0.19
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2009 2016
dbSNP: rs579459
rs579459
0.784 0.107 9 133278724 regulatory region variant C/T snp 0.20
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2014
dbSNP: rs780094
rs780094
0.699 0.286 2 27518370 intron variant T/C snp 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 < 0.001 1 2010 2016