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: rs1333049
rs1333049
0.614 0.520 9 22125504 intron variant G/C snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 1.000 9 2007 2020
dbSNP: rs4977574
rs4977574
0.695 0.520 9 22098575 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 5 2011 2018
dbSNP: rs9349379
rs9349379
0.732 0.200 6 12903725 intron variant A/G snv 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 4 2011 2019
dbSNP: rs10757278
rs10757278
0.620 0.520 9 22124478 intron variant A/G snv 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 3 2008 2016
dbSNP: rs11066280
rs11066280
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 3 2012 2013
dbSNP: rs1333042
rs1333042
0.827 0.120 9 22103814 intron variant A/G snv 0.63
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 3 2011 2016
dbSNP: rs17465637
rs17465637
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 1.000 3 2007 2013
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: 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: rs1122608
rs1122608
0.763 0.120 19 11052925 intron variant G/T snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2016
dbSNP: rs12524865
rs12524865
1.000 0.040 6 133875536 intron variant C/A snv 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2012
dbSNP: rs12526453
rs12526453
0.827 0.160 6 12927312 intron variant C/G snv 0.27
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2017
dbSNP: rs1333048
rs1333048
0.683 0.320 9 22125348 intron variant A/C snv 0.44
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2016
dbSNP: rs1412444
rs1412444
0.851 0.120 10 89243170 intron variant C/T snv 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2011
dbSNP: rs17114046
rs17114046
0.925 0.040 1 56500678 intron variant A/G snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2011
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: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 2 2012 2013
dbSNP: rs4773144
rs4773144
0.827 0.080 13 110308365 intron variant A/G snv 0.42
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 2 2011 2016
dbSNP: rs6511720
rs6511720
0.790 0.120 19 11091630 intron variant G/T snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.720 1.000 2 2011 2016
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: rs6922269
rs6922269
0.807 0.200 6 150931849 intron variant G/A snv 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 2 2007 2014
dbSNP: rs9982601
rs9982601
0.851 0.080 21 34226827 intron variant C/T snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 2 2011 2017
dbSNP: rs10217586
rs10217586
1.000 0.040 9 22121350 intron variant A/T snv 0.52
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10218795
rs10218795
HJV
1.000 0.040 1 146018957 intron variant G/A snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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