Disease: Obesity
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 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
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 6
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs7638110
MRPS22
1.000 0.080 3 139185143 intron variant G/T snv 9.4E-02 2
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 5
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 3
rs9568867 1.000 0.080 13 53533217 intron variant G/A snv 0.13 2
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 8
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 8
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 5
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42 3
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 8
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 6
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 3
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 2
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11