Source: GWASCAT

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 30
rs3847858 12 51924594 downstream gene variant A/T snv 8.9E-02 3
rs4823308
LINC01589
22 45604058 downstream gene variant T/A snv 0.38 3
rs67145503
AK1
9 127866245 downstream gene variant T/A snv 0.21 3
rs7045087
ACO1 ; DDX58
9 32455264 downstream gene variant T/C snv 0.33 3
rs551238
EPO
0.925 0.160 7 100723905 downstream gene variant G/T snv 0.62 2
rs9260313
HLA-A
6 29949108 downstream gene variant T/C snv 0.42 2
rs2032314
LOC105372790
21 33982222 downstream gene variant T/C snv 0.86 1
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs11730623 4 69020433 upstream gene variant A/T snv 0.66 2
rs1340817 13 28656444 upstream gene variant A/G snv 0.47 2
rs149823406 7 100716851 upstream gene variant C/T snv 4.6E-03 2
rs6967414 7 6710127 upstream gene variant G/A snv 0.29 2
rs9614727 22 45629162 upstream gene variant G/A snv 0.11 2
rs554093579 7 100537063 upstream gene variant A/C snv 5.5E-03 1
rs56235845
RGS14
5 177371039 splice region variant T/G snv 0.36 0.42 2
rs62482253
GNB2
7 100677821 splice region variant G/A snv 2.6E-03 2.8E-03 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs2732480
ZNF641
12 48342520 3 prime UTR variant C/A snv 0.39 3