Disease: Coronary heart disease
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1263173 0.925 0.080 11 116810292 downstream gene variant G/A snv 0.53 3
rs181937009
LOC107986652 ; LOC100507477
0.925 0.040 6 140064258 intron variant A/G snv 0.23 3
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 4
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 4
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 4
rs12272004 1.000 0.040 11 116733008 TF binding site variant C/A snv 9.8E-02 5
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 5
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 5
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 5
rs3846663
HMGCR ; CERT1
0.882 0.120 5 75359901 intron variant C/T snv 0.35 5
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs6754295 1.000 0.040 2 20983311 regulatory region variant T/G snv 0.27 6
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 7
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 7
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 8
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 8
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 8