Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 9
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 8
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 7
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 7
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 7
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 6
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 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
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
rs2497318 0.827 0.120 10 92672243 upstream gene variant C/A;T snv 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
rs4917129 0.807 0.240 7 50283578 intergenic variant T/C snv 0.51 6
rs559928 0.827 0.120 11 64382898 intergenic variant T/C snv 0.77 6
rs6426833 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 6