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: rs11754384
rs11754384
1.000 0.040 6 26322757 upstream gene variant T/G snv 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs12646936
rs12646936
1.000 0.040 4 135841484 intergenic variant T/G snv 0.59
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs2395174
rs2395174
0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs5943057
rs5943057
1.000 0.040 X 110695977 intron variant T/G snv 0.50
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs6754295
rs6754295
1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs7134341
rs7134341
1.000 0.040 12 119143326 intron variant T/G snv 8.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs7808424
rs7808424
1.000 0.040 7 117427768 intron variant T/G snv 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs9261588
rs9261588
1.000 0.040 6 30243030 intron variant T/G snv 0.92
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs944797
rs944797
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 3 2011 2013
dbSNP: rs2681492
rs2681492
0.925 0.040 12 89619312 intron variant T/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs2743941
rs2743941
1.000 0.040 6 29787674 upstream gene variant T/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs4939883
rs4939883
1.000 0.040 18 49640844 TF binding site variant T/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs68191
rs68191
1.000 0.040 6 33512961 regulatory region variant T/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs6903982
rs6903982
1.000 0.040 6 27577965 intergenic variant T/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs501120
rs501120
0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 3 2007 2012
dbSNP: rs11066001
rs11066001
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 2 2012 2013
dbSNP: rs17228212
rs17228212
0.807 0.160 15 67166301 intron variant T/C snv 0.21
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 2 2007 2012
dbSNP: rs3782886
rs3782886
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 2 2012 2013
dbSNP: rs3798220
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2013
dbSNP: rs6725887
rs6725887
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2014
dbSNP: rs10401969
rs10401969
0.776 0.240 19 19296909 intron variant T/C snv 0.10
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2016
dbSNP: rs10811661
rs10811661
0.724 0.400 9 22134095 intergenic variant T/C snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.710 1.000 1 2011 2011
dbSNP: rs11024074
rs11024074
0.925 0.040 11 16895672 intron variant T/C snv 0.29
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs11112992
rs11112992
1.000 0.040 12 106435501 intron variant T/C snv 0.20
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs11191548
rs11191548
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011