Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1759645 6 34227089 TF binding site variant C/T snv 0.71 1
rs17690232 4 54368658 regulatory region variant C/A;G snv 1
rs1776897 6 34227234 regulatory region variant G/T snv 0.80 1
rs1809889 12 124316680 downstream gene variant T/C snv 0.62 1
rs1814175 11 49537620 intergenic variant T/A;C snv 1
rs1878528 4 81263080 intergenic variant A/G snv 0.39 1
rs1950500 14 24361644 upstream gene variant T/C snv 0.68 1
rs2079795 17 61419288 regulatory region variant T/A;C snv 1
rs2145270 20 6641038 regulatory region variant C/T snv 0.61 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs2145998 10 79361940 regulatory region variant T/A snv 0.48 1
rs2154319 1 41280098 intron variant T/C snv 0.15 1
rs227724 17 56701456 intergenic variant A/T snv 0.31 1
rs2326458 16 84954073 intergenic variant C/A snv 0.67 1
rs2353398 4 144601606 intron variant T/A snv 0.66 1
rs2553026 2 217258925 upstream gene variant G/A;C snv 1
rs2554380 15 83647132 intergenic variant C/T snv 0.85 1
rs2580816 2 231933256 regulatory region variant C/T snv 0.28 1
rs2597513 1.000 0.040 3 13514336 regulatory region variant C/T snv 0.88 1
rs2629046 2 224183027 intergenic variant T/C snv 0.53 1
rs2665838 17 63889105 downstream gene variant C/A;G;T snv 1
rs26868 16 2199375 upstream gene variant T/A;C snv 1
rs2778031 1.000 0.040 9 88220811 intergenic variant T/A;C snv 1
rs2780226 6 34231315 regulatory region variant C/T snv 0.80 1
rs281379 1.000 0.040 19 48711017 downstream gene variant G/A snv 0.38 1