Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 10
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 9
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 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
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 8
rs6495308
CHRNA3
0.851 0.160 15 78615314 intron variant T/C snv 0.29 8
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 8
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 8
rs2036534
HYKK
0.827 0.080 15 78534606 3 prime UTR variant T/C snv 0.26 8
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 8
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
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
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7
rs1994016
ADAMTS7
0.851 0.160 15 78787892 intron variant C/T snv 0.30 7
rs3743078
CHRNA3
0.807 0.160 15 78602417 intron variant C/A;G snv 7
rs938682
CHRNA3
0.851 0.080 15 78604205 intron variant G/A snv 0.72 7
rs13280604
CHRNB3 ; LOC105379396
0.851 0.160 8 42704443 5 prime UTR variant G/A snv 0.62 7
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7