Source: ALL
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 0.15 272
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 18
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 17
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 13
rs578776
CHRNA3
0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 13
rs667282
CHRNA5
0.790 0.120 15 78571130 intron variant T/C snv 0.28 13
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 10
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 10
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 10