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: rs10030552
rs10030552
MAML3
4 140051110 intron variant C/A snv 0.24
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs10031466
rs10031466
TRIML2
4 188094248 intron variant G/A snv 0.56
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs1003858
rs1003858
PAPPA
9 116202676 intron variant G/C snv 1.1E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs10041657
rs10041657
FER
5 108816727 intron variant G/A snv 0.23
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs1004787
rs1004787
LINC01833
2 44931952 intron variant G/A snv 0.68
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs1014667
rs1014667
NRXN1
2 50521617 intron variant G/A;C snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs10160101
rs10160101
BEND7
10 13507462 intron variant G/C snv 0.30
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
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: rs10195252
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs10243383
rs10243383
RAPGEF5
1.000 0.040 7 22242733 intron variant C/T snv 0.51
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs10269774
rs10269774
CDK6
7 92624658 intron variant G/A snv 0.36
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs10279261
rs10279261
EXOC4
7 133905093 intron variant G/A snv 0.69
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs10488693
rs10488693
DAGLA
11 61717684 intron variant C/T snv 6.0E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs10759883
rs10759883
LINC00476
9 95790481 intron variant C/T snv 0.58
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs10780649
rs10780649
LOC101927575
9 84088646 intron variant T/G snv 0.64
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs10783615
rs10783615
HOXC12 ; LOC105369775
12 53955989 intron variant G/A snv 0.71
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs10842707
rs10842707 		12 26318431 intron variant C/G;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs10914684
rs10914684
PHC2
1 33329971 intron variant G/A snv 0.25
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs10923712
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs10928235
rs10928235
TEX41
1.000 0.080 2 144920547 intron variant A/T snv 0.18
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs10958852
rs10958852
PTPRD
9 10060843 intron variant C/T snv 4.5E-04
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs10968576
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs10991437
rs10991437
CT70
9 104973639 intron variant C/A snv 9.0E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs11030104
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs1106529
rs1106529
TBX15
1 118988874 intron variant G/A snv 0.77
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017