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: rs7801190
rs7801190
1.000 0.040 7 100860471 non coding transcript exon variant C/G snv 9.9E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 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: rs3824755
rs3824755
0.925 0.120 10 102836092 intron variant G/A;C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs12411886
rs12411886
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs12413409
rs12413409
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2011 2014
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: 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: 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: rs2385168
rs2385168
1.000 0.040 7 104438209 intron variant C/A;T snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012
dbSNP: rs2515629
rs2515629
1.000 0.040 9 104832083 intron variant A/G snv 0.16
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs4149268
rs4149268
1.000 0.040 9 104884939 intron variant C/T snv 0.46
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs3890182
rs3890182
0.925 0.120 9 104885374 intron variant G/A;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs3905000
rs3905000
0.925 0.080 9 104894789 intron variant G/A snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs1883025
rs1883025
0.807 0.120 9 104902020 intron variant C/T snv 0.28
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2011 2011
dbSNP: rs11112992
rs11112992
1.000 0.040 12 106435501 intron variant T/C snv 0.20
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2013 2013
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: 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: rs12740374
rs12740374
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.810 1.000 1 2011 2018
dbSNP: rs629301
rs629301
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 1 2012 2016
dbSNP: rs646776
rs646776
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.830 1.000 3 2011 2016
dbSNP: rs599839
rs599839
0.724 0.360 1 109279544 downstream gene variant G/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.850 1.000 3 2007 2018
dbSNP: rs2338104
rs2338104
1.000 0.040 12 109457363 non coding transcript exon variant C/G snv 0.58
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: rs922971
rs922971
1.000 0.040 8 109817880 intergenic variant G/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2012 2012