Source: BEFREE

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 80
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 18
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 17
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 14
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 9
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 8
rs7204609
FTO
0.827 0.200 16 53799693 intron variant T/C snv 0.14 6
rs11075995
FTO
0.882 0.080 16 53821379 intron variant A/T snv 0.77 5
rs1477196
FTO
0.851 0.200 16 53774346 intron variant A/G snv 0.71 5
rs16953002
FTO
0.882 0.080 16 54080912 intron variant G/A snv 0.19 4
rs8057044
FTO
0.882 0.080 16 53778702 intron variant G/A snv 0.54 4
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv 4
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42 3
rs9926289
FTO
0.882 0.160 16 53786591 intron variant G/A snv 0.41 3
rs7195539
FTO
0.925 0.080 16 53825246 intron variant A/G snv 7.3E-02 3
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 3
rs1588413
FTO
0.882 0.200 16 54115620 3 prime UTR variant G/A snv 0.14 3
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 3
rs745616565
FTO
1.000 0.200 16 53873855 missense variant G/A snv 1.6E-05 2.1E-05 2
rs121918214
FTO
1.000 0.200 16 53873837 missense variant G/A snv 4.0E-06 7.0E-06 2
rs781028867
FTO
1.000 0.200 16 53873846 missense variant C/A;T snv 4.0E-06 2
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 2
rs11076023
FTO
0.925 0.120 16 54118136 3 prime UTR variant A/T snv 0.49 2
rs56094641
FTO
0.925 0.160 16 53772541 intron variant A/G;T snv 2