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: rs11642421
rs11642421 		16 23738456 intergenic variant G/C snv 0.21
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs1164598
rs1164598
HS6ST3
13 96449317 intron variant A/C;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs116571008
rs116571008
LINC00448
13 62709905 intron variant C/G snv 3.6E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs1167827
rs1167827
HIP1
7 75533848 3 prime UTR variant G/A snv 0.37
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs116885154
rs116885154
LINC00469 ; LINC02092
17 73788236 intron variant G/C snv 6.1E-03
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs11708245
rs11708245
TAFA4
3 68747005 intron variant G/A snv 0.28
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs117178387
rs117178387
AMD1 ; CDK19
6 110815877 non coding transcript exon variant T/C snv 3.2E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs1174864
rs1174864 		7 53059866 intergenic variant G/A snv 0.52
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: rs11771982
rs11771982
PLXNA4
7 132617489 intron variant C/T snv 0.12
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11779675
rs11779675
XKR6
8 10980951 intron variant G/A snv 0.28
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs117898875
rs117898875 		3 84223836 regulatory region variant T/C snv 3.3E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11808210
rs11808210 		1 227327348 intergenic variant G/A snv 6.7E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11844846
rs11844846
LINC02326 ; LOC107984685
14 29018462 intron variant A/G snv 0.48
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11864332
rs11864332 		16 12883205 downstream gene variant C/T snv 9.2E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs11872397
rs11872397
ZNF407
18 74823326 intron variant G/A snv 0.25
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11876432
rs11876432 		18 45089460 regulatory region variant C/G snv 0.18
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11878604
rs11878604 		19 40827379 intron variant T/C snv 0.14
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2016 2016
dbSNP: rs11919456
rs11919456
BDH1
3 197538563 3 prime UTR variant A/G snv 0.31
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs12016871
rs12016871
MTIF3
13 27443645 intron variant C/T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
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: rs12030183
rs12030183 		1 41295548 intron variant T/C snv 0.28
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs12042107
rs12042107 		1 90730619 downstream gene variant T/C snv 0.59
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs12048049
rs12048049
TGFB2
1 218423955 intron variant C/G snv 0.37
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs12053870
rs12053870
LOC105374060
3 118583668 intron variant T/G snv 0.45
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019