Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs802791 0.851 0.160 6 106121395 intron variant T/C snv 0.75 4
rs906868 0.925 0.120 2 30225478 intergenic variant G/T snv 0.53 4
rs911263 0.851 0.200 14 68286876 intron variant C/T snv 0.57 4
rs9268832 0.882 0.160 6 32460012 non coding transcript exon variant T/C snv 0.61 0.59 4
rs9275328 0.851 0.240 6 32699045 intergenic variant C/T snv 0.16 4
rs1051792 0.851 0.240 6 31411200 missense variant G/A snv 0.34 0.35 5
rs12531711 0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs12537 0.827 0.280 22 30027471 3 prime UTR variant C/T snv 0.40 5
rs13238352 0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 5
rs17849502 0.827 0.240 1 183563445 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 3.4E-02 5
rs2239804 0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs2251396 0.827 0.240 6 31396930 upstream gene variant G/A snv 0.24 5
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs2431098 0.827 0.240 5 160460329 intron variant A/G;T snv 5
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 5
rs2858331 0.827 0.240 6 32713500 upstream gene variant A/G snv 0.42 5
rs2900180 0.827 0.280 9 120944104 regulatory region variant T/A;C snv 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3129939 0.827 0.360 6 32368989 intron variant A/G snv 0.14 5
rs3130320 0.851 0.160 6 32255481 intron variant T/C snv 0.68 5
rs3130340 0.851 0.200 6 32276850 intron variant T/C snv 0.25 5
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs4085613 0.827 0.160 1 152577542 downstream gene variant T/G snv 0.59 5
rs560051377 0.851 0.320 1 161624624 missense variant G/A;C snv 4.0E-06; 2.8E-05 5
rs6659932 0.827 0.240 1 67336688 intron variant A/C snv 0.81 5