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: rs12535004
rs12535004
7 115307058 intergenic variant T/C snv 0.28
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12600773
rs12600773
17 52258612 intergenic variant C/T snv 0.26
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12662631
rs12662631
6 93132728 intergenic variant C/T snv 0.23
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs1267068
rs1267068
2 161155624 intron variant T/G snv 0.26
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
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: rs12757183
rs12757183
1 216747031 intron variant T/C snv 0.15
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12764388
rs12764388
10 102653628 non coding transcript exon variant G/A snv 8.8E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12787182
rs12787182
11 59423338 5 prime UTR variant A/G snv 0.25
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12825376
rs12825376
12 120742136 intron variant C/T snv 7.2E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12895462
rs12895462
14 77149098 intron variant T/C snv 0.14
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12930834
rs12930834
16 72917728 intron variant A/C snv 0.16
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs12997449
rs12997449
2 178174845 intergenic variant A/G snv 8.2E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs13065007
rs13065007
3 117803865 intron variant T/A snv 0.24
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs13160204
rs13160204
5 158307754 intergenic variant G/A;T snv 0.31
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs13187930
rs13187930
5 61088344 intron variant T/C snv 0.76
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs13234909
rs13234909
7 1827295 intron variant G/A snv 0.33
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs13237637
rs13237637
7 3463575 intron variant G/C snv 0.40
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs13258512
rs13258512
8 91765205 intron variant A/G snv 0.44
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs13357015
rs13357015
5 80967584 intron variant G/A snv 0.69
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs13396935
rs13396935
2 653195 intergenic variant G/A snv 0.18
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs1368550
rs1368550
2 103462197 intergenic variant T/C snv 0.43
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs1373129
rs1373129
9 99391416 intergenic variant A/C;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs138045331
rs138045331
2 122082314 intron variant A/C snv 3.9E-03
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs141980369
rs141980369
1.000 0.040 6 118888344 intron variant G/A snv 6.1E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019