Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 4
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 3
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 7
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 5
rs849140
JAZF1
0.851 0.240 7 28144083 intron variant T/C snv 0.58 3
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 5
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 2
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 1
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 1
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 4
rs13180
IREB2
0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 3
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 3
rs6495308
CHRNA3
0.851 0.160 15 78615314 intron variant T/C snv 0.29 2
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 2
rs1994016
ADAMTS7
0.851 0.160 15 78787892 intron variant C/T snv 0.30 1