Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs13389219 1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs10195252 0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs6795735 0.882 0.120 3 64719689 intron variant C/A;G;T snv 3