Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11669133
SMARCA4
1.000 0.040 19 10981463 intron variant G/A snv 4.2E-02 2
rs11671653
DNM2
1.000 0.040 19 10727810 intron variant G/A;T snv 2
rs12042319
DOCK7
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 6
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
rs13015955 1.000 0.040 2 22599287 intergenic variant G/A snv 0.18 2
rs13161895
RNF130
1.000 0.040 5 180044201 intron variant C/T snv 0.12 2
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 6
rs2254287
COL11A2
1.000 0.040 6 33176171 intron variant C/A;G;T snv 3
rs4844614
CR1L
1.000 0.040 1 207701830 intron variant G/C;T snv 3
rs5031002
AR
1.000 0.040 X 67722783 intron variant G/A snv 1.5E-02 1.5E-02 3
rs503662 1.000 0.040 2 21191270 intergenic variant T/C snv 0.63 3
rs6102059
LOC102724968
1.000 0.040 20 40600144 intergenic variant C/T snv 0.33 3
rs7569328 1.000 0.040 2 20901018 intergenic variant C/T snv 5.7E-02 2
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs12654264
HMGCR
0.925 0.120 5 75352778 intron variant A/T snv 0.38 7
rs6544713
ABCG8
0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 5
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 5
rs6756629
ABCG5 ; ABCG8
0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 5
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11