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: rs11066001
rs11066001
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 2 2012 2013
dbSNP: rs2074356
rs2074356
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 2 2012 2013
dbSNP: rs3782886
rs3782886
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 2 2012 2013
dbSNP: rs651007
rs651007
0.851 0.160 9 133278431 upstream gene variant T/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 2 2011 2011
dbSNP: rs1004467
rs1004467
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs10217586
rs10217586
1.000 0.040 9 22121350 intron variant A/T snv 0.52
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10218795
rs10218795
HJV
1.000 0.040 1 146018957 intron variant G/A snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs10431335
rs10431335
1.000 0.040 12 128194523 upstream gene variant C/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10468017
rs10468017
0.851 0.120 15 58386313 intron variant C/T snv 0.24
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs10484404
rs10484404
1.000 0.040 6 28087717 intron variant C/T snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs10498725
rs10498725
1.000 0.040 6 25454787 intron variant C/T snv 0.17
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs10503669
rs10503669
0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1051730
rs1051730
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs10738609
rs10738609
1.000 0.040 9 22114496 intron variant A/C;G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10738610
rs10738610
0.882 0.120 9 22123767 intron variant A/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10757272
rs10757272
0.851 0.160 9 22088261 intron variant C/T snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10757275
rs10757275
1.000 0.040 9 22106226 intron variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10757277
rs10757277
1.000 0.040 9 22124451 intron variant A/G snv 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10757279
rs10757279
0.925 0.040 9 22124631 intron variant A/G snv 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10847434
rs10847434
1.000 0.040 12 127676248 intergenic variant C/T snv 0.29
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10849917
rs10849917
1.000 0.040 12 110919270 intron variant T/A snv 0.13
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10858300
rs10858300
1.000 0.040 9 134950654 intergenic variant C/T snv 0.24
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
dbSNP: rs10923931
rs10923931
0.925 0.120 1 119975336 intron variant G/T snv 0.17
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs10946398
rs10946398
0.827 0.160 6 20660803 intron variant A/C snv 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs10947460
rs10947460
1.000 0.040 6 33860457 intergenic variant G/A snv 0.15
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012