Disease: Smoking
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12317176
CCDC92 ; DNAH10
12 123920171 intron variant T/C snv 0.39 3
rs12493901
FNDC3B
3 172204265 intron variant G/A snv 0.37 3
rs12731372 1 118310352 regulatory region variant C/T snv 0.19 3
rs12991495
DNMT3A
2 25263901 intron variant T/C snv 0.22 3
rs13083798
PBRM1
3 52615732 intron variant A/G snv 0.51 3
rs13191362
PRKN
6 162612318 intron variant A/G snv 8.7E-02 3
rs17405819 8 75894349 intergenic variant T/C snv 0.24 3
rs1879529
ACAN
15 88871064 intron variant G/T snv 0.28 3
rs1928295 9 117616205 intergenic variant T/C snv 0.45 3
rs2245368
DTX2P1-UPK3BP1-PMS2P11 ; LOC105375361
7 76978826 non coding transcript exon variant C/T snv 0.80 3
rs2365389
FHIT
3 61250788 intron variant C/T snv 0.56 3
rs4141278 7 25817905 intergenic variant T/C snv 0.16 3
rs4239436
CABLES1
18 23151966 intron variant A/G snv 0.81 3
rs4542783
MYO1F
19 8577276 non coding transcript exon variant T/C snv 0.53 0.52 3
rs4765219
CCDC92
12 123955563 intron variant C/A;T snv 3
rs6090583
EYA2
20 46930192 intron variant A/C;G snv 3
rs6437061
DIS3L2
2 232320342 intron variant A/C snv 0.56 3
rs6715793
LTBP1
2 33154196 intron variant C/T snv 0.43 3
rs6772896
CEP63 ; ANAPC13
3 134484505 intron variant C/T snv 0.68 3
rs6804842
RARB
3 25064946 intron variant A/G snv 0.53 3
rs7164727 15 72801650 downstream gene variant C/G;T snv 3
rs754133
HOXC6 ; HOXC4 ; HOXC5
12 54025136 intron variant G/A;C snv 3
rs7766106
RSPO3
6 127133993 intron variant C/T snv 0.44 3
rs7830933
LOC107986930
8 23745811 intron variant A/G snv 0.24 3
rs8042543
KLF13
15 31416060 intron variant C/G;T snv 3