Disease: Smoking Behaviors
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
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
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
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 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
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 10
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7
rs849140
JAZF1
0.851 0.240 7 28144083 intron variant T/C snv 0.58 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 6