Disease: Smoking
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113196862 11 58315137 downstream gene variant C/T snv 4.0E-02 2
rs113288656
PTCHD1-AS
X 22417389 intron variant T/C snv 2.1E-02 2
rs113441626
NR2E3
15 71814833 3 prime UTR variant C/G snv 3.4E-03 2
rs113496184
WWOX
16 79006207 intron variant G/C;T snv 2
rs113626797 2 81068213 regulatory region variant T/C snv 2.0E-02 2
rs113991851 4 12025243 intergenic variant C/T snv 2.1E-02 2
rs114114977
LOC105375005
6 29318457 intergenic variant G/A;C snv 2
rs114167782
LOC105375467 ; CFTR ; WNT2
7 117299233 intron variant C/T snv 3.0E-02 2
rs114622739 4 77975394 intergenic variant C/T snv 2.2E-02 2
rs114780919
GRAMD1C
3 113931599 intron variant C/T snv 4.5E-02 2
rs114951929
TNK2
3 195864852 intron variant G/A snv 5.6E-02 2
rs115205687
PLCB1
20 8915129 intron variant G/T snv 2.2E-02 2
rs115219852
USP34
2 61424393 intron variant G/A snv 2.6E-02 2
rs115536975
DOCK1
10 126973570 intron variant A/T snv 4.5E-02 2
rs116383923
SNX29
16 12381345 intron variant C/G snv 2
rs11642421 16 23738456 intergenic variant G/C snv 0.21 2
rs116571008
LINC00448
13 62709905 intron variant C/G snv 3.6E-02 2
rs116885154
LINC02092 ; LINC00469
17 73788236 intron variant G/C snv 6.1E-03 2
rs11708245
TAFA4
3 68747005 intron variant G/A snv 0.28 2
rs117178387
AMD1 ; CDK19
6 110815877 non coding transcript exon variant T/C snv 3.2E-02 2
rs11864332 16 12883205 downstream gene variant C/T snv 9.2E-02 2
rs11919456
BDH1
3 197538563 3 prime UTR variant A/G snv 0.31 2
rs12048049
TGFB2
1 218423955 intron variant C/G snv 0.37 2
rs12127195 1 221136075 upstream gene variant G/A snv 0.33 2
rs12143789
TBX15
1 118954531 intron variant G/C snv 0.13 2