Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
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
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
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 10
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 9
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 8
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs3743078
CHRNA3
0.807 0.160 15 78602417 intron variant C/A;G snv 7
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7
rs931794
HYKK
0.851 0.080 15 78533838 3 prime UTR variant G/A;C snv 7
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv 6
rs3813565
LOC105370913 ; CHRNB4
0.851 0.080 15 78727268 splice region variant G/A;T snv 6
rs7177514
CHRNA3
0.882 0.080 15 78615064 intron variant C/G;T snv 6
rs8042059
CHRNA3
0.882 0.080 15 78615517 intron variant A/C;T snv 6
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv 6
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2656069
IREB2
0.882 0.080 15 78453365 intron variant C/G;T snv 5
rs684513
CHRNA5
0.925 0.080 15 78566058 intron variant C/G;T snv 5
rs10842707 12 26318431 intron variant C/G;T snv 4
rs11072768
CHRNB4
0.882 0.080 15 78637136 intron variant T/C;G snv 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4