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
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
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
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 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
rs4854344 1.000 0.080 2 638144 regulatory region variant G/T snv 0.82 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
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 4
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 4
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 4
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 4
rs13180
IREB2
0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 4