Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1468758 9 111044802 intergenic variant C/T snv 0.23 1
rs1490384 6 126530014 intron variant C/G;T snv 1
rs1490388 6 126514509 intron variant C/G;T snv 1
rs153750 5 171754233 intergenic variant T/G snv 0.71 1
rs1549519 17 55680426 intergenic variant T/A;C snv 1
rs1582931 5 123321505 intergenic variant G/A;T snv 1
rs1636255 7 2853170 regulatory region variant C/A;T snv 1
rs1662840 4 81235255 intergenic variant C/T snv 0.38 1
rs17038182 1 118325782 intergenic variant G/C snv 0.25 1
rs1738475 1 23210398 regulatory region variant C/G snv 0.49 1
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
rs1863190 1.000 0.080 2 217263429 non coding transcript exon variant A/T snv 0.53 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