Disease: Obesity
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 7
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 7
rs4833407
ALPK1
1.000 0.080 4 112390634 intron variant C/A;T snv 2
rs6711012 1.000 0.080 2 624034 intergenic variant G/A;C;T snv 2
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 12
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 8
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs9299
HOXB5 ; HOXB3 ; HOXB-AS3
1.000 0.080 17 48592068 3 prime UTR variant C/A;T snv 2
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs13447324
MC4R
1.000 0.080 18 60372245 stop gained G/T snv 6.8E-05 1.3E-04 2
rs17150703 1.000 0.080 8 9888288 intergenic variant G/A snv 8.5E-02 2
rs7638110
MRPS22
1.000 0.080 3 139185143 intron variant G/T snv 9.4E-02 2
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs9568867 1.000 0.080 13 53533217 intron variant G/A snv 0.13 2
rs13078807
CADM2
0.925 0.120 3 85835000 intron variant A/G snv 0.15 4
rs2207139 1.000 0.080 6 50877777 intergenic variant A/G snv 0.16 4
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 7
rs11208659
LEPR
1.000 0.080 1 65513597 intron variant T/A;C snv 0.17 2
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 8