Source: GWASDB

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
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 7
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
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
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
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 5
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 4
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 4
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 4
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 4
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 4
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 4
rs9935401
FTO
0.925 0.120 16 53782926 intron variant G/A snv 0.40 3
rs8051591
FTO
0.925 0.120 16 53782840 intron variant A/G snv 0.40 3
rs11642841
FTO
0.925 0.120 16 53811575 intron variant C/A;G snv 3
rs11075989
FTO
0.925 0.120 16 53785965 intron variant C/A;T snv 3
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 3
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 3
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 3
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv 3
rs7190492
FTO
1.000 0.080 16 53794840 intron variant A/G snv 0.68 3