Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs181937009
LOC107986652 ; LOC100507477
0.925 0.040 6 140064258 intron variant A/G snv 0.23 3
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 5
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs3812316
MLXIPL
0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 7
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
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
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
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
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 5