Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 7
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 5
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 4
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 3
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 3
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 3
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 3
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 3
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 3
rs56094641
FTO
0.925 0.160 16 53772541 intron variant A/G;T snv 2
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 1
rs11642841
FTO
0.925 0.120 16 53811575 intron variant C/A;G snv 1
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 1
rs62048402
FTO
0.882 0.200 16 53769311 intron variant G/A snv 0.31 1
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 1
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 1