Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 5
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 3
rs2656069
IREB2
0.882 0.080 15 78453365 intron variant C/G;T snv 3
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 3
rs3813565
LOC105370913 ; CHRNB4
0.851 0.080 15 78727268 splice region variant G/A;T snv 3
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 3
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 3
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv 3
rs10508503 1.000 0.080 10 16257952 intergenic variant C/A;T snv 2
rs1021070
CHRNB4
15 78654521 intron variant C/A;G snv 1
rs11072766
IREB2
15 78479204 intron variant C/G;T snv 1
rs11072768
CHRNB4
0.882 0.080 15 78637136 intron variant T/C;G snv 1
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 1
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 1
rs11633519
LOC112268142 ; LOC105370913 ; CHRNB4
15 78707210 intron variant A/G;T snv 1
rs12531858
PDE1C
7 32300487 intron variant C/A;G snv 1
rs12903295
IREB2
15 78486630 intron variant A/C;G;T snv 1
rs12910627
LOC112268142 ; CHRNB4 ; LOC105370913
15 78702591 intron variant G/A;C snv 1
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv 1
rs1443512 12 53948900 downstream gene variant A/C;T snv 1
rs1451239 8 42691399 intergenic variant G/A;T snv 1