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: rs6437740
rs6437740
BBX
3 107746970 intron variant T/C snv 0.25
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2009 2009
dbSNP: rs1051730
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 4 2008 2010
dbSNP: rs1329650
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2010 2010
dbSNP: rs215614
rs215614
PDE1C
7 32307723 intron variant G/A snv 0.62
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2010 2010
dbSNP: rs3025343
rs3025343 		9 133613233 non coding transcript exon variant G/A snv 7.0E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2010 2010
dbSNP: rs3733829
rs3733829
EGLN2 ; RAB4B-EGLN2
0.882 0.120 19 40804666 non coding transcript exon variant A/G snv 0.28
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2010 2010
dbSNP: rs4105144
rs4105144 		0.827 0.160 19 40852719 intron variant T/C snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2010 2010
dbSNP: rs6474412
rs6474412 		0.925 0.120 8 42695355 upstream gene variant C/T snv 0.64
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2010 2010
dbSNP: rs1451240
rs1451240 		0.925 0.080 8 42691568 intergenic variant A/G snv 0.64
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2012 2012
dbSNP: rs1678618
rs1678618 		10 72046530 intergenic variant A/G snv 0.39
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2012 2012
dbSNP: rs2036527
rs2036527 		0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2012 2012
dbSNP: rs3101457
rs3101457
C1orf100
1 244369912 intron variant G/A snv 0.80
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2012 2012
dbSNP: rs547843
rs547843 		15 26178900 regulatory region variant C/G;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2012 2012
dbSNP: rs667282
rs667282
CHRNA5
0.790 0.120 15 78571130 intron variant T/C snv 0.28
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2012 2012
dbSNP: rs8102683
rs8102683 		19 40857860 intron variant T/C snv 0.75
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2012 2012
dbSNP: rs848353
rs848353 		1.000 0.080 7 108908603 upstream gene variant A/G snv 0.14
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2012 2012
dbSNP: rs55958997
rs55958997
CHRNB4
1.000 0.040 15 78623530 upstream gene variant C/A snv 0.32
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2014 2014
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: rs1014667
rs1014667
NRXN1
2 50521617 intron variant G/A;C snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs10440708
rs10440708 		5 173223484 downstream gene variant A/G snv 4.3E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
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: rs10501157
rs10501157
TRAF6
11 36485319 3 prime UTR variant T/C snv 1.6E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs10856789
rs10856789 		2 19581401 intergenic variant T/A;C snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs10912872
rs10912872 		1 171387110 intergenic variant G/T snv 0.38
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015