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: rs7865618
rs7865618
0.878 0.071 9 22031006 non coding transcript exon variant G/A,T snp 0.70
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2012 2017
dbSNP: rs974819
rs974819
0.923 0.036 11 103789839 intron variant T/A,C snp 0.65
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2013
dbSNP: rs9939609
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2016
dbSNP: rs9349379
rs9349379
0.801 0.071 6 12903725 intron variant A/G snp 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 4 2011 2012
dbSNP: rs11066280
rs11066280
0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 3 2012 2013
dbSNP: rs11556924
rs11556924
0.784 0.143 7 130023656 missense variant C/A,T snp 4.0E-06; 0.28 0.26
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 3 2011 2014
dbSNP: rs1333042
rs1333042
0.923 0.071 9 22103814 intron variant A/G snp 0.61
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 3 2012 2013
dbSNP: rs944797
rs944797
0.878 0.143 9 22115287 intron variant T/C snp 0.48
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 3 2012 2013
dbSNP: rs12524865
rs12524865
1.000 0.036 6 133875536 intron variant C/A snp 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 2 2011 2012
dbSNP: rs1412444
rs1412444
0.923 0.036 10 89243170 intron variant C/T snp 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 2 2011 2012
dbSNP: rs17114046
rs17114046
0.923 0.036 1 56500678 intron variant A/G snp 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 2 2011 2011
dbSNP: rs1746048
rs1746048
0.878 0.036 10 44280376 regulatory region variant C/T snp 0.24
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 2 2011 2011
dbSNP: rs4773144
rs4773144
0.923 0.036 13 110308365 intron variant A/G snp 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 2 2011 2012
dbSNP: rs6725887
rs6725887
0.878 0.036 2 202881162 intron variant T/C snp 9.1E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 2 2011 2014
dbSNP: rs9818870
rs9818870
0.878 0.036 3 138403280 3 prime UTR variant C/A,T snp 6.4E-05; 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 2 2009 2014
dbSNP: rs9982601
rs9982601
0.878 0.036 21 34226827 intron variant C/T snp 0.16
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 2 2011 2014
dbSNP: rs10401969
rs10401969
0.801 0.214 19 19296909 intron variant T/C snp 9.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1 2011 2016
dbSNP: rs10953541
rs10953541
1.000 0.036 7 107604100 intron variant C/T snp 0.18
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1 2011 2011
dbSNP: rs11066015
rs11066015
0.923 0.107 12 111730205 intron variant G/A snp 1.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1 2013 2013
dbSNP: rs11752643
rs11752643
0.923 0.107 6 32701596 intergenic variant C/T snp 2.2E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1 2012 2012
dbSNP: rs12200560
rs12200560
1.000 0.036 6 96632322 intergenic variant A/G snp 0.36
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1 2012 2012
dbSNP: rs1231206
rs1231206
1.000 0.036 17 2222311 intron variant G/A snp 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1 2011 2011
dbSNP: rs12413409
rs12413409
0.846 0.071 10 102959339 intron variant G/A snp 9.3E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1 2011 2014
dbSNP: rs12449964
rs12449964
1.000 0.036 17 17641390 intergenic variant C/T snp 0.35
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1 2011 2014
dbSNP: rs12734338
rs12734338
0.923 0.107 1 202500595 intron variant T/C snp
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1 2013 2013