Source: ALL

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: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.810 1.000 7 2011 2018
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.800 1.000 3 2010 2017
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.800 1.000 1 2012 2012
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.730 1.000 5 2009 2012
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.710 1.000 2 2009 2014
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 2 2011 2015
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		0.700 1.000 1 2011 2011
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		0.700 1.000 1 2011 2011
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 1 2011 2011
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0008677
Disease: Bronchitis, Chronic
Bronchitis, Chronic 		0.700 1.000 1 2014 2014
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0728877
Disease: Serum albumin level
Serum albumin level 		0.700 1.000 1 2012 2012
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.030 1.000 3 2010 2012
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.030 1.000 3 2010 2012
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2010 2010
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2010 2010
dbSNP: rs12914385
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2018 2018