Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
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
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
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
rs12654264
HMGCR
0.925 0.120 5 75352778 intron variant A/T snv 0.38 7
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 5
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
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
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
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 17