Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 5
rs2030746
LOC105373585
0.925 0.120 2 120551912 downstream gene variant C/T snv 0.44 5
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs1277930
PSRC1
1 109279521 downstream gene variant G/A snv 0.63 4
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 4
rs11577931 1 109278262 downstream gene variant A/G snv 5.5E-02 3
rs12097137 1 101243889 downstream gene variant G/A;T snv 3
rs17645031
MYBPHL
1 109292316 downstream gene variant C/T snv 7.9E-02 3
rs235216
TNFRSF1B
1 12209567 downstream gene variant C/A;G;T snv 3
rs3093208
CYP4F2
19 15877772 downstream gene variant A/G snv 4.0E-02 3
rs314253
DLG4
17 7188331 downstream gene variant T/C snv 0.37 3
rs55882046 1 109277359 downstream gene variant C/T snv 6.7E-02 3
rs655246 1 109289661 downstream gene variant A/C;G snv 3
rs7952037 11 102379653 downstream gene variant C/T snv 1.9E-02 3
rs289742
CETP
16 56983850 downstream gene variant C/G snv 0.80 2
rs597078
USP1
1 62452186 downstream gene variant G/A;C;T snv 0.43 2