Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
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
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 4
rs9939973
FTO
1.000 0.080 16 53766656 intron variant G/A snv 0.42 3