Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1022261
rs1022261 		4 35474678 intergenic variant A/C snv 0.52
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs10919388
rs10919388 		1 170403362 intergenic variant A/C snv 0.71
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs12854631
rs12854631 		X 58297412 intergenic variant A/C snv 2.7E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs12930834
rs12930834
ZFHX3
16 72917728 intron variant A/C snv 0.16
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs138045331
rs138045331
LOC105373592
2 122082314 intron variant A/C snv 3.9E-03
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs139214349
rs139214349 		4 29168543 intron variant A/C snv 1.4E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs144528474
rs144528474
WDPCP
2 63650871 intron variant A/C snv 8.1E-04
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs147168872
rs147168872
SOS2
14 50173277 intron variant A/C snv 5.0E-03
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs1856293
rs1856293 		6 133159801 intergenic variant A/C snv 0.56
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs2820292
rs2820292
NAV1 ; IPO9-AS1
1 201815159 intron variant A/C snv 0.48
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs6437061
rs6437061
DIS3L2
2 232320342 intron variant A/C snv 0.56
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs6452791
rs6452791 		5 88475276 intron variant A/C snv 0.55
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs72724928
rs72724928
LINGO2
9 28024196 intron variant A/C snv 3.3E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs72923818
rs72923818
DYM
18 49157384 intron variant A/C snv 4.0E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs12022778
rs12022778
ELAVL4
1 50138323 intron variant A/C;G snv 0.21
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs1221976
rs1221976
DCC
18 52469766 intron variant A/C;G snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs12286929
rs12286929 		0.925 0.080 11 115151684 intergenic variant A/C;G snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs142383097
rs142383097
DFFA
1.000 0.040 1 10461101 3 prime UTR variant A/C;G snv 2.0E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs189798510
rs189798510 		17 14811500 intergenic variant A/C;G snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs2734971
rs2734971 		6 29866672 intron variant A/C;G snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs2945731
rs2945731 		8 133627845 intergenic variant A/C;G snv 4.9E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs4947642
rs4947642 		7 51797912 intergenic variant A/C;G snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs55828312
rs55828312
CHRNB3
8 42734459 intron variant A/C;G snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs6090583
rs6090583
EYA2
20 46930192 intron variant A/C;G snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs7897478
rs7897478 		1.000 0.040 10 29945955 intergenic variant A/C;G snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019