Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 23
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 13
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 12
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 11
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
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
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 9
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 9
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 8
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 8
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 8
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7