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: rs10503023
rs10503023 		18 59165543 intergenic variant G/A snv 0.21
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2018 2018
dbSNP: rs10751226
rs10751226 		11 73601207 upstream gene variant C/G;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
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: rs10804591
rs10804591 		3 129615390 intergenic variant C/A snv 0.63
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: 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
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: rs10919388
rs10919388 		1 170403362 intergenic variant A/C snv 0.71
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
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: rs10929925
rs10929925 		2 6015425 intergenic variant C/A;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs10938397
rs10938397 		0.851 0.200 4 45180510 intergenic variant A/G snv 0.37
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs10952199
rs10952199 		7 1625703 downstream gene variant C/T snv 0.41
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: rs10970595
rs10970595
LOC105376011
9 31910766 intergenic variant C/T snv 8.2E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
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: rs10994943
rs10994943
LINC02625
10 61831655 intergenic variant T/G snv 0.34
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11019935
rs11019935 		11 88441800 intergenic variant C/A;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
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
dbSNP: rs11066971
rs11066971 		12 114165055 intergenic variant C/T snv 0.10
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019