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: rs6265
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 2 2010 2019
dbSNP: rs10020574
rs10020574
LOC105374553
4 28061344 intergenic variant C/G snv 0.78
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
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: 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: 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: rs1022261
rs1022261 		4 35474678 intergenic variant A/C snv 0.52
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
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: rs10252114
rs10252114 		7 122315414 upstream gene variant T/C snv 0.37
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
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: rs10461104
rs10461104 		4 27488957 intergenic variant G/A snv 0.68
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
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: 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: 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: 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: 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: 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: 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: rs11066971
rs11066971 		12 114165055 intergenic variant C/T snv 0.10
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs1108879
rs1108879
SDK1
7 3516500 intron variant G/A snv 0.61
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs1109480
rs1109480
CABP1
12 120645476 intron variant G/A snv 0.31
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11134672
rs11134672
RANBP17
5 170968816 intron variant G/A snv 0.60
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11165528
rs11165528
LINC02790
1 95967238 intron variant C/T snv 0.52
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11166986
rs11166986 		8 140646056 TF binding site variant G/A;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11210892
rs11210892 		1.000 0.040 1 43634413 intergenic variant G/A snv 0.51
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11255908
rs11255908 		10 8760949 intergenic variant T/G snv 0.35
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019