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: 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: rs114969316
rs114969316
1.000 0.040 6 88460643 intergenic variant A/G snv 1.6E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs1150668
rs1150668
6 28162011 intron variant T/G snv 0.58
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs115319209
rs115319209
1.000 0.040 14 75298968 downstream gene variant G/A snv 1.0E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs1164598
rs1164598
13 96449317 intron variant A/C;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
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: rs11771982
rs11771982
7 132617489 intron variant C/T snv 0.12
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs11779675
rs11779675
8 10980951 intron variant G/A snv 0.28
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs11783093
rs11783093
1.000 0.040 8 27567832 intron variant C/T snv 0.11
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
14 29018462 intron variant A/G snv 0.48
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs11872397
rs11872397
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: rs12022778
rs12022778
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: 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: 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: rs12053870
rs12053870
3 118583668 intron variant T/G snv 0.45
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12211126
rs12211126
6 66839558 intergenic variant T/C snv 0.28
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: rs12456711
rs12456711
18 280897 intergenic variant A/G snv 0.22
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs1246265
rs1246265
9 84146830 regulatory region variant T/C snv 0.76
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12476173
rs12476173
2 117490138 intergenic variant G/A snv 0.48
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12517438
rs12517438
5 30841947 intergenic variant T/G snv 0.40
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019