Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12198986 6 7719826 regulatory region variant G/A snv 0.37 1
rs12474201 2 46694146 upstream gene variant G/A snv 0.30 1
rs1257763 9 94131663 intron variant A/G snv 0.97 1
rs12735613 1 118341350 intergenic variant G/A snv 0.22 1
rs13227860 1.000 0.040 7 22114836 downstream gene variant G/A snv 0.26 1
rs13336428 16 1482462 downstream gene variant G/A snv 0.53 1
rs1401796 17 56762398 intergenic variant C/A snv 0.54 1
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
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
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