Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012411 1.000 0.120 6 30364778 upstream gene variant T/G snv 0.32 1
rs10774654 1.000 0.120 12 112525756 intergenic variant A/G snv 0.20 1
rs10795791 0.925 0.200 10 6066377 upstream gene variant A/G snv 0.40 1
rs10807113 1.000 0.120 6 32754409 upstream gene variant C/A;G snv 1
rs10850053 1.000 0.120 12 112539973 regulatory region variant T/C snv 0.19 1
rs11160219 1.000 0.120 14 94869154 regulatory region variant A/G snv 0.75 1
rs11624318 1.000 0.120 14 94839675 intergenic variant C/A snv 0.15 1
rs12251307 1.000 0.120 10 6081532 intergenic variant C/T snv 0.18 1
rs12444268 1.000 0.120 16 20331250 upstream gene variant T/A snv 0.22 1
rs12453507 0.925 0.200 17 39896954 intergenic variant C/G;T snv 1
rs1358030 0.925 0.120 10 106363841 intergenic variant G/A snv 0.57 1
rs1456988 0.925 0.160 14 98021670 intergenic variant G/T snv 0.61 1
rs148735424 1.000 0.120 6 32697982 intergenic variant -/TTCGTC;TTCGTCAGAC delins 1
rs154978 1.000 0.120 6 32931519 downstream gene variant C/T snv 0.54 1
rs17208888 1.000 0.120 6 32411729 upstream gene variant G/A snv 8.0E-02 1
rs188245 1.000 0.120 6 32988199 regulatory region variant A/G snv 0.44 1
rs1977090 1.000 0.120 6 33217801 downstream gene variant C/T snv 0.11 1
rs206769 1.000 0.120 6 32993327 regulatory region variant C/T snv 0.20 1
rs206777 1.000 0.120 6 32984769 downstream gene variant G/A snv 0.66 1
rs2394990 1.000 0.120 6 31372782 intron variant C/A snv 0.56 1
rs2442749 1.000 0.120 6 31384263 upstream gene variant T/C snv 0.24 1
rs2517485 1.000 0.120 6 31106324 downstream gene variant C/A;T snv 1
rs2523864 1.000 0.120 6 31050769 upstream gene variant C/T snv 0.47 1
rs2844697 1.000 0.120 6 30964532 upstream gene variant C/T snv 0.44 1
rs2858308 1.000 0.120 6 32702223 downstream gene variant G/T snv 0.10 1