Disease: Obesity
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1412239
LINGO2
0.925 0.120 9 28425517 intron variant C/G snv 0.26 2
rs1514177
TNNI3K ; FPGT-TNNI3K ; LRRC53
1.000 0.080 1 74525718 intron variant C/G snv 0.49 2
rs11127485 1.000 0.080 2 632028 intergenic variant C/T snv 0.85 2
rs1514174
LRRC53 ; FPGT-TNNI3K ; TNNI3K
1.000 0.080 1 74527379 intron variant C/T snv 0.44 2
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6
rs2206277
TFAP2B
0.925 0.080 6 50830813 intron variant C/T snv 0.19 4
rs2531995
ADCY9
1.000 0.080 16 3963466 3 prime UTR variant C/T snv 0.45 7
rs7141420
NRXN3
1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 3
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34 6
rs12149832
FTO
0.851 0.120 16 53808996 intron variant G/A snv 0.31 7
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 7
rs17150703 1.000 0.080 8 9888288 intergenic variant G/A snv 8.5E-02 2
rs7132908
FAIM2
1.000 0.080 12 49869365 3 prime UTR variant G/A snv 0.31 4
rs9568867 1.000 0.080 13 53533217 intron variant G/A snv 0.13 2
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42 3
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 8
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 7
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
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs13447324
MC4R
1.000 0.080 18 60372245 stop gained G/T snv 6.8E-05 1.3E-04 2
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 7
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 6