Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs41295061 0.790 0.360 10 6072697 upstream gene variant C/A snv 6.1E-02 8
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 7
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 7
rs9392504 0.827 0.120 6 412802 downstream gene variant G/A snv 0.44 7
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs11117433 0.827 0.160 16 85985910 upstream gene variant G/A;C;T snv 6
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 6
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs114558062 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 5
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5
rs55984493 0.851 0.040 13 99118074 intergenic variant A/T snv 0.15 5
rs6927172 0.851 0.120 6 137681038 intron variant C/A;G;T snv 5
rs6933404 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 5
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs970987 0.851 0.040 9 21585266 regulatory region variant C/A snv 0.55 5
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 5
rs10202630 0.882 2 190398199 intergenic variant T/C snv 0.52 4