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
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 8
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
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 4
rs2197089 0.925 0.080 8 19968862 downstream gene variant G/A snv 0.61 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 3
rs12097137 1 101243889 downstream gene variant G/A;T snv 3
rs235216
TNFRSF1B
1 12209567 downstream gene variant C/A;G;T snv 3
rs2967605
RAB11B
0.925 0.040 19 8404854 downstream gene variant C/T snv 0.20 3
rs3916027
LPL
8 19967357 downstream gene variant G/A snv 0.31 3
rs4921683
LPL
8 19967557 downstream gene variant T/A snv 0.14 3
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 3
rs9644636
LPL
8 19967385 downstream gene variant T/A;G snv 3
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 2
rs2814944 1.000 0.040 6 34585020 downstream gene variant G/A snv 0.20 2
rs289742
CETP
16 56983850 downstream gene variant C/G snv 0.80 2
rs289743
CETP
16 56983884 downstream gene variant G/A;C;T snv 2
rs289744
CETP
16 56984190 downstream gene variant G/T snv 0.61 2
rs34989676 5 148830704 downstream gene variant G/A snv 1.4E-02 2
rs3922628 12 122724748 downstream gene variant T/A;C snv 2