Disease: Smoking Behaviors
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 7
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 5
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs17700144 1.000 0.080 18 60144750 intron variant G/A snv 0.14 4
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 4
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 4
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 4
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 4
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 3
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 3
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 3
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 3
rs4752856
MTCH2
1.000 0.040 11 47626490 intron variant G/A snv 0.28 3
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 3