Disease: Obesity
Source: CURATED ×
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 25
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 7
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 6
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 6
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 5
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 5
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 5
rs663129 0.882 0.160 18 60171168 intergenic variant G/A snv 0.24 4
rs11075989
FTO
0.925 0.120 16 53785965 intron variant C/A;T snv 3
rs11642841
FTO
0.925 0.120 16 53811575 intron variant C/A;G snv 3
rs8051591
FTO
0.925 0.120 16 53782840 intron variant A/G snv 0.40 3
rs9935401
FTO
0.925 0.120 16 53782926 intron variant G/A snv 0.40 3