Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs188096 1.000 0.080 13 103052694 missense variant A/C snv 0.85 0.89 1
rs7229639 0.763 0.080 18 48924606 intron variant A/G snv 0.87 5
rs2278008 0.851 0.160 5 33989413 missense variant C/T snv 0.70 0.74 4
rs3087967 0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 1
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1391441 0.763 0.240 4 105207603 intron variant G/A snv 0.70 1
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 8
rs10808555 0.925 0.080 8 127397266 intron variant G/A snv 0.65 5
rs1126667 0.776 0.280 17 6999441 missense variant A/G snv 0.60 0.62 8
rs7013278 0.776 0.080 8 127402647 intron variant T/C snv 0.59 1
rs704017 0.776 0.080 10 79059375 intron variant A/G snv 0.55 1
rs13251096 1.000 0.080 8 58505225 downstream gene variant A/G snv 0.53 1
rs11874392 0.763 0.080 18 48926786 intron variant A/T snv 0.50 2
rs3789243 0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs7023329 0.790 0.160 9 21816529 intron variant A/G snv 0.50 8
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 14
rs10246939 0.851 0.240 7 141972804 missense variant T/C snv 0.49 0.47 4
rs1726866 0.925 0.120 7 141972905 missense variant G/A snv 0.50 0.47 2
rs713598 0.851 0.160 7 141973545 missense variant C/G snv 0.46 0.44 6
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 15
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 18
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187