Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs181937009
LOC107986652 ; LOC100507477
0.925 0.040 6 140064258 intron variant A/G snv 0.23 3
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 6
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 7
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 6
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 5
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60