Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 5
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 4
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 4
rs1508595 0.851 0.240 12 88592239 intron variant G/A;T snv 3
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 3
rs305061 0.851 0.280 16 85942053 intron variant C/A;T snv 3
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 3
rs4624820 0.851 0.240 5 142302223 regulatory region variant G/A snv 0.55 3
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 3
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 2
rs11228565 0.882 0.160 11 69211113 regulatory region variant G/A snv 0.16 2
rs1154865 0.882 0.160 12 73596057 intergenic variant C/G snv 0.22 2
rs1327301 0.882 0.160 X 51467205 downstream gene variant C/T snv 0.29 2
rs16886165 0.882 0.160 5 56727256 intergenic variant T/C;G snv 0.22 2
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 2
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 2
rs29232 0.925 0.240 6 29643654 intergenic variant C/T snv 0.39 2
rs3123078 0.882 0.160 10 46070851 regulatory region variant G/A snv 0.55 2
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 2
rs4242384 0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88 2
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 2
rs4699052 0.925 0.200 4 103216633 intergenic variant C/T snv 0.44 2
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 2
rs5759167 0.851 0.160 22 43104206 TF binding site variant G/T snv 0.40 2
rs5945572 0.882 0.160 X 51486831 downstream gene variant A/G snv 2