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: rs1412444
rs1412444
0.851 0.120 10 89243170 intron variant C/T snv 0.37
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2011
dbSNP: rs17114046
rs17114046
0.925 0.040 1 56500678 intron variant A/G snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 2 2011 2011
dbSNP: rs2259816
rs2259816
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2009 2011
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: 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: 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: 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: rs10811661
rs10811661
0.724 0.400 9 22134095 intergenic variant T/C snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.710 1.000 1 2011 2011
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: 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: rs11014166
rs11014166
0.882 0.040 10 18419869 intron variant A/T snv 0.27
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.710 1.000 1 2010 2011
dbSNP: rs11024074
rs11024074
0.925 0.040 11 16895672 intron variant T/C snv 0.29
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1111875
rs1111875
0.776 0.360 10 92703125 intergenic variant C/T snv 0.36
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs11191548
rs11191548
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1153188
rs1153188
0.925 0.120 12 54705212 intergenic variant T/A snv 0.76
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1165668
rs1165668
1.000 0.040 12 103924218 intron variant G/A snv 0.71
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1165669
rs1165669
1.000 0.040 12 103924394 intron variant A/G snv 0.71
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs11668477
rs11668477
0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs11669133
rs11669133
1.000 0.040 19 10981463 intron variant G/A snv 4.2E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs11671653
rs11671653
1.000 0.040 19 10727810 intron variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs11924705
rs11924705
1.000 0.040 3 162443828 intergenic variant T/C snv 0.33
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs12091564
rs12091564
1.000 0.040 1 146039391 upstream gene variant A/C;G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011