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: 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: 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: rs10755578
rs10755578
LPA
0.925 0.040 6 160548706 intron variant C/G snv 0.44 0.42
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2009 2009
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: rs10953541
rs10953541
1.000 0.040 7 107604100 intron variant C/T snv 0.17
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs11057830
rs11057830
0.851 0.040 12 124822507 intron variant G/A snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.710 1.000 1 2017 2019
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: rs11066015
rs11066015
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2013 2013
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 1 2012 2013
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 1 2011 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: 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 2 2011 2017
dbSNP: rs11638352
rs11638352
0.925 0.040 15 44000939 intron variant C/A;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs11752643
rs11752643
0.925 0.120 6 32701596 downstream gene variant C/T snv 2.3E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2012 2012
dbSNP: rs117714106
rs117714106
0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs11915606
rs11915606
BTD
0.925 0.040 3 15633655 intron variant T/G snv 3.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
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 2 2011 2017
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: rs12290663
rs12290663
0.925 0.040 11 26141193 intergenic variant G/A snv 5.7E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs12310617
rs12310617
0.851 0.120 12 3060327 intergenic variant C/T snv 0.11
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs1231206
rs1231206
1.000 0.040 17 2222311 intron variant G/A snv 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs12369179
rs12369179
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2014
dbSNP: rs12420422
rs12420422
0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs12449964
rs12449964
1.000 0.040 17 17641390 regulatory region variant C/T snv 0.36
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2014