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: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2015 2015
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
Squamous cell carcinoma of the head and neck 		0.010 1.000 1 2015 2015
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2016 2016
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2015 2015
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2015 2015
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		0.010 1.000 1 2011 2011
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
Squamous cell carcinoma of esophagus 		0.010 1.000 1 2018 2018
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2012 2012
dbSNP: rs3813867
rs3813867
CYP2E1 ; LOC107984284
0.732 0.240 10 133526101 intron variant G/A;C snv
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2013 2013