Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs997050266 0.851 0.120 19 45423352 missense variant T/A;C snv 1.4E-05 4
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9904341 0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs9838411 0.925 0.080 3 179169899 intron variant G/A snv 0.25 2
rs9668337 1.000 0.080 12 26273405 non coding transcript exon variant G/A snv 0.55 1
rs9639594 1.000 0.080 7 29139570 intron variant G/A snv 0.20 1
rs9600103 1.000 0.080 13 73237742 intergenic variant A/T snv 0.33 1
rs944050 0.827 0.280 14 64233327 splice region variant T/C snv 9.5E-02 7.9E-02 5
rs937213 1.000 0.080 15 40029923 intron variant T/C snv 0.31 3
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs9261204 0.790 0.200 6 30037466 intron variant A/G snv 0.17 9
rs911162 1.000 0.080 20 56391393 intron variant A/C;G snv 1
rs892119 0.925 0.080 19 40254165 intron variant C/T snv 0.19 2
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 18
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs882380 1.000 0.080 17 48216874 intron variant C/A snv 0.52 1
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs876660943 0.882 0.240 2 47806359 splice donor variant G/T snv 7.0E-06 5
rs876658932 0.807 0.400 16 68801726 stop gained C/G;T snv 7
rs872267 1.000 0.080 3 128169224 intron variant G/A snv 0.43 1
rs864622149 0.851 0.160 22 28710005 splice donor variant C/A;G;T snv 5
rs864622121 1.000 0.080 2 47475228 frameshift variant GT/- del 2
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104