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: 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: rs11066001
rs11066001
0.878 0.143 12 111681367 intron variant T/C snp 1.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 2 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: rs1333048
rs1333048
0.821 0.071 9 22125348 intergenic variant A/C snp 0.43
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 2 2012 2013
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: rs2074356
rs2074356
0.821 0.214 12 112207597 intron variant G/A snp 8.6E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 2 2012 2013
dbSNP: rs3782886
rs3782886
0.784 0.250 12 111672685 synonymous variant T/C snp 1.9E-02 1.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 2 2012 2013
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: rs651007
rs651007
0.821 0.143 9 133278431 regulatory region variant T/A,C snp 0.20
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 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: rs1004467
rs1004467
0.878 0.107 10 102834750 non coding transcript exon variant A/G snp 0.15 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1 2011 2011
dbSNP: rs10217586
rs10217586
1.000 0.036 9 22121350 intergenic variant A/T snp 0.51
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1 2013 2013
dbSNP: rs10218795
rs10218795
HJV
1.000 0.036 1 146018957 intron variant G/A snp 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1 2012 2012
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: rs10431335
rs10431335
1.000 0.036 12 128194523 intergenic variant C/A,T snp 6.4E-05; 0.32
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1 2013 2013
dbSNP: rs10468017
rs10468017
0.846 0.107 15 58386313 intron variant C/T snp 0.25
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1 2011 2011
dbSNP: rs10484404
rs10484404
1.000 0.036 6 28087717 intron variant C/T snp 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1 2012 2012