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: rs59876823
rs59876823
13 100082270 intron variant C/A snv 0.10
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs3783177
rs3783177
13 100499106 intron variant T/G snv 0.17
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs10958852
rs10958852
9 10060843 intron variant C/T snv 4.5E-04
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs239245
rs239245
6 100642501 intron variant C/A snv 0.56
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs182466621
rs182466621
2 100730839 intergenic variant G/A;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs140386998
rs140386998
X 100959983 downstream gene variant C/T snv 3.7E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs60866311
rs60866311
2 100975599 non coding transcript exon variant T/G snv 4.1E-02 7.2E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs7901883
rs7901883
10 101427081 intron variant G/A;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs17396340
rs17396340
1 10226118 intron variant G/A;C snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs13107325
rs13107325
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs3862030
rs3862030
10 102567827 intron variant A/G snv 0.45
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
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: rs7917772
rs7917772
10 102727686 3 prime UTR variant G/A;C snv 0.46
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs17151637
rs17151637
8 10295572 intron variant C/G;T snv
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs7092200
rs7092200
10 103085115 3 prime UTR variant T/C snv 0.42
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs11191560
rs11191560
10 103109281 intron variant T/C snv 8.4E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs71417845
rs71417845
14 103210903 downstream gene variant C/G snv 1.7E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs1430065
rs1430065
2 103240616 intergenic variant C/T snv 0.25
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs71471272
rs71471272
10 103245744 upstream gene variant G/A snv 4.5E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs1628768
rs1628768
10 103253237 intergenic variant T/C 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: rs41427747
rs41427747
4 103999322 intron variant G/T snv 5.6E-02
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2015 2015
dbSNP: rs17348216
rs17348216
5 104588673 intron variant C/T snv 0.15
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2019 2019
dbSNP: rs142383097
rs142383097
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: rs395962
rs395962
6 104949543 intron variant T/G snv 0.72
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017