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: rs1014667
rs1014667
2 50521617 intron variant G/A;C snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs1016287
rs1016287
2 59078490 intron variant T/A;C;G snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs10751226
rs10751226
11 73601207 upstream gene variant C/G;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs10842707
rs10842707
12 26318431 intron variant C/G;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs10856789
rs10856789
2 19581401 intergenic variant T/A;C snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs10929925
rs10929925
2 6015425 intergenic variant C/A;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs11019935
rs11019935
11 88441800 intergenic variant C/A;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs11166986
rs11166986
8 140646056 TF binding site variant G/A;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs11205277
rs11205277
1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs1128249
rs1128249
1.000 0.080 2 164672114 intron variant G/C;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs113029345
rs113029345
19 40864271 intron variant T/C snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2016 2016
dbSNP: rs113496184
rs113496184
16 79006207 intron variant G/C;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs1136998
rs1136998
2 43888044 3 prime UTR variant T/A;C snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs114114977
rs114114977
6 29318457 intergenic variant G/A;C snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs116383923
rs116383923
16 12381345 intron variant C/G snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs1164598
rs1164598
13 96449317 intron variant A/C;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs117582141
rs117582141
10 92804854 intergenic variant T/A;C snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs12016871
rs12016871
13 27443645 intron variant C/T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs12036147
rs12036147
1.000 0.040 1 239835413 intron variant A/G;T snv
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: rs12608504
rs12608504
19 18278325 upstream gene variant A/G;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs12690535
rs12690535
2 225394657 intergenic variant G/A;C snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs1271272
rs1271272
2 207090753 intron variant G/A;C snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12914385
rs12914385
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017