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: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 1.000 2 2008 2019
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 1.000 2 2008 2019
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C0153382
Disease: Malignant neoplasm of oropharynx
Malignant neoplasm of oropharynx 		0.010 1.000 1 2012 2012
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		0.010 1.000 1 2011 2011
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2008 2008
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C0001418
Disease: Adenocarcinoma
Adenocarcinoma 		0.010 1.000 1 2008 2008
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C0017638
Disease: Glioma
Glioma 		0.010 < 0.001 1 2014 2014
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C2349952
Disease: Oropharyngeal Carcinoma
Oropharyngeal Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2008 2008
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
Squamous cell carcinoma of the head and neck 		0.010 1.000 1 2012 2012
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2008 2008
dbSNP: rs3136038
rs3136038
ERCC4
0.763 0.200 16 13919522 upstream gene variant C/T snv 0.36
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		0.010 1.000 1 2011 2011