Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs12180309 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 4
rs55702914 0.925 0.080 2 197349672 intergenic variant C/G snv 0.37 4
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1824024 0.851 0.160 7 136958947 intron variant C/A snv 0.65 4
rs1535255 0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs72737330 0.925 0.080 1 216600151 intron variant T/C snv 0.15 4
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs6691840 0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 5
rs11568817 0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs130058 0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs11825659 0.925 0.080 11 133925624 intron variant A/G snv 0.12 4
rs58598658 0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs2273816 0.851 0.080 13 49719920 intron variant G/A;C snv 4