Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1013209 8 24258791 intergenic variant C/T snv 0.28 1
rs10231759 7 150815084 regulatory region variant T/C snv 0.41 1
rs10472828 5 32888712 non coding transcript exon variant C/T snv 0.40 1
rs1052483 2 219069626 non coding transcript exon variant G/T snv 0.13 1
rs10748128 12 69433878 intergenic variant G/T snv 0.42 1
rs10799445 1 227724182 upstream gene variant A/C snv 0.27 1
rs11118346 1 219570377 intergenic variant C/T snv 0.38 1
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 1
rs1173727 5 32830415 intergenic variant T/C snv 0.66 1
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
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
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