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: rs460976
rs460976
0.851 0.120 21 41463567 downstream gene variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs4704221
rs4704221
0.851 0.120 5 75463358 intron variant T/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs4714955
rs4714955
1.000 0.040 6 12903203 intron variant C/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2014 2014
dbSNP: rs478442
rs478442
0.851 0.120 2 21176344 intergenic variant G/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs4905014
rs4905014
0.851 0.120 14 92945686 intron variant G/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs514659
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2011
dbSNP: rs6841581
rs6841581
0.882 0.080 4 147480038 upstream gene variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2014 2014
dbSNP: rs7081476
rs7081476
0.851 0.120 10 26969741 intergenic variant G/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs7136259
rs7136259
1.000 0.040 12 89687411 intron variant T/A;C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2012 2012
dbSNP: rs765547
rs765547
0.827 0.160 8 20008763 intergenic variant G/A;C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs7865618
rs7865618
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 1 2011 2017
dbSNP: rs9369640
rs9369640
0.851 0.080 6 12901209 intron variant C/A;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2014 2014
dbSNP: rs9508025
rs9508025
0.925 0.040 13 28409926 intron variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2013 2013
dbSNP: rs974819
rs974819
0.807 0.080 11 103789839 intron variant T/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2012
dbSNP: rs3883013
rs3883013
1.000 0.040 15 84545426 intron variant T/C snv 5.6E-05
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2013 2013
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: rs76863441
rs76863441
0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.760 0.714 1 2009 2017
dbSNP: rs192427471
rs192427471
0.925 0.040 4 124644124 intergenic variant C/T snv 2.4E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs148121703
rs148121703
0.925 0.040 4 47371654 intron variant TGT/- delins 2.6E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs189889864
rs189889864
0.925 0.040 9 104634643 downstream gene variant G/A snv 2.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
dbSNP: rs671
rs671
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 1.000 1 2010 2020
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: rs151269874
rs151269874
0.925 0.040 16 75549741 intron variant C/T snv 6.2E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2017 2017
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