Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174550 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 6
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 5
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 5
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 5
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 5
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 5
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs11558471 1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs2568958 0.882 0.160 1 72299433 intron variant G/A;C snv 5
rs10913469 1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs7498665 0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 4
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 4
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4