Disease: Smoking Behaviors
Source: INFERRED ×
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 25
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 12
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 8
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 7
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 7
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 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
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 6
rs12902602
LOC112268142 ; CHRNB4
15 78675059 intron variant A/G snv 0.28 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 5
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 5
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 5
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 4
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 4