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: rs4689388
rs4689388
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs5219
rs5219
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs564398
rs564398
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2018
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.710 1.000 1 2011 2016
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: rs10455872
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 1 2011 2018
dbSNP: rs10757274
rs10757274
0.701 0.320 9 22096056 intron variant A/G snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 1.000 1 2008 2016
dbSNP: rs2237892
rs2237892
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs2383206
rs2383206
0.742 0.320 9 22115027 intron variant A/G snv 0.49
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.720 1.000 1 2008 2013
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: rs579459
rs579459
0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2014
dbSNP: rs864745
rs864745
0.763 0.320 7 28140937 intron variant T/C snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
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: 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: rs2259816
rs2259816
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2009 2011
dbSNP: rs1004467
rs1004467
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs12190287
rs12190287
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2011 2017
dbSNP: rs1333045
rs1333045
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs3764261
rs3764261
0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs3846662
rs3846662
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs4506565
rs4506565
0.790 0.280 10 112996282 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2016
dbSNP: rs11556924
rs11556924
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 3 2011 2017
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: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 3 2011 2016
dbSNP: rs11206510
rs11206510
0.763 0.240 1 55030366 intergenic variant T/A;C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2013