Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 9
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs7136716 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 6
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 5
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 12
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs35237252 1.000 0.040 8 20012760 intergenic variant C/A;T snv 0.24 2
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 9
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5