Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12042319
DOCK7
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 6
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 6
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 6
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs3761740
HMGCR
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02 4
rs3846663
HMGCR ; CERT1
0.882 0.120 5 75359901 intron variant C/T snv 0.35 7
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18