Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 6
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 6
rs2050392 0.827 0.120 10 30402574 downstream gene variant G/A snv 0.45 6
rs2143178 0.827 0.120 22 39264824 intron variant T/C snv 0.19 6
rs2538470 0.827 0.120 7 148523356 intergenic variant A/G snv 0.61 6
rs4243971 0.827 0.120 20 32261714 intergenic variant T/G snv 0.64 6
rs4703855 0.827 0.120 5 72398072 regulatory region variant C/T snv 0.24 6
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 6
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 6
rs71559680 0.827 0.120 6 21430497 intergenic variant TAG/CAT mnv 6
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 6
rs9889296 0.827 0.120 17 34243528 intergenic variant G/A snv 0.33 6
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 5
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 5