Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs1883025 0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs13389219 1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs8070723 0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs10808546 8 125483576 intron variant C/T snv 0.39 4
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs10195252 0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs17249754 0.882 0.120 12 89666809 intron variant G/A snv 0.15 3
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 3
rs6795735 0.882 0.120 3 64719689 intron variant C/A;G;T snv 3
rs7647305 1.000 0.080 3 186116501 intron variant T/C snv 0.74 3
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs987237 0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs9931989 16 28894763 intron variant G/C snv 0.68 3
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 2
rs1876829 1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 2
rs2287019 1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 2
rs634869 6 139510620 intron variant T/A;C snv 2
rs718314 0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs7776725 1.000 0.080 7 121393067 intron variant T/C snv 0.28 2