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
rs7531118
LOC105378797
1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
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
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 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
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 6
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 5
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 5
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
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
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 5
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 5
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 5
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 4
rs12969709 1.000 0.080 18 60192330 upstream gene variant C/A snv 0.21 4
rs13078807
CADM2
0.925 0.120 3 85835000 intron variant A/G snv 0.15 4