Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs2075291
APOA5 ; ZPR1
0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7819412
XKR6
0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16