Source: GWASCAT

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: 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 1 2011 2016
dbSNP: rs2980853
rs2980853
0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs9351814
rs9351814
0.882 0.040 6 71484004 intergenic variant A/C snv 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2014 2014
dbSNP: rs2943634
rs2943634
0.763 0.200 2 226203364 intergenic variant A/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 1 2007 2012
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 2 2007 2013
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: 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 2 2011 2018
dbSNP: rs17114036
rs17114036
0.851 0.120 1 56497149 intron variant A/G snv 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2014
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: 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: rs11065987
rs11065987
0.807 0.280 12 111634620 intergenic variant A/G snv 0.29
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2014 2014
dbSNP: rs12200560
rs12200560
1.000 0.040 6 96632322 intergenic variant A/G snv 0.36
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2012 2012
dbSNP: rs12579302
rs12579302
0.851 0.120 12 89656726 intron variant A/G snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
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 1 2011 2016
dbSNP: rs144972973
rs144972973
0.925 0.040 15 44272494 intergenic variant A/G snv 1.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs147204125
rs147204125
0.925 0.040 14 73609035 intron variant A/G snv 9.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs149232047
rs149232047
0.925 0.040 6 126276990 intergenic variant A/G snv 1.5E-04
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs181937009
rs181937009
0.925 0.040 6 140064258 intron variant A/G snv 0.23
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs2281727
rs2281727
0.882 0.080 17 2214651 intron variant A/G snv 0.38
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2014 2014
dbSNP: rs261332
rs261332
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs3782889
rs3782889
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2013 2013
dbSNP: rs3825807
rs3825807
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs4420638
rs4420638
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2009 2016
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 1 2011 2016
dbSNP: rs4803750
rs4803750
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016