rs8042374, CHRNA3

N. diseases: 9
Source: CURATED ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
173 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.710 1.000 3 2008 2012
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
404 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.710 1.000 1 2009 2014
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
237 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.710 1.000 1 2008 2011
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
1629 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.700 1.000 3 2014 2017
Smoking Behaviors
CUI: C1519383
Disease: Smoking Behaviors
742 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.700 1.000 3 2010 2010
Child Development Disorders, Pervasive
379 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.700 1.000 1 2017 2017
Forced expiratory volume function
CUI: C0016529
Disease: Forced expiratory volume function
1169 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.700 1.000 1 2015 2015
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
174 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.700 1.000 1 2010 2010
response to bronchodilator
CUI: C3548479
Disease: response to bronchodilator
1106 0.807 0.200 15 78615690 intron variant A/G snv 0.29 0.700 1.000 1 2015 2015