Source: ALL
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.
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.763 0.160 7 55181312 missense variant G/T snv 0.740 1.000 11 2004 2018
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.763 0.160 7 55181312 missense variant G/T snv 0.050 1.000 5 2006 2018
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.763 0.160 7 55181312 missense variant G/T snv 0.700 1.000 2 2006 2014
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.763 0.160 7 55181312 missense variant G/T snv 0.700 1.000 2 2012 2013
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.763 0.160 7 55181312 missense variant G/T snv 0.010 1.000 1 2017 2017
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.763 0.160 7 55181312 missense variant G/T snv 0.010 1.000 1 2016 2016
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.763 0.160 7 55181312 missense variant G/T snv 0.010 1.000 1 2013 2013
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.763 0.160 7 55181312 missense variant G/T snv 0.010 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.763 0.160 7 55181312 missense variant G/T snv 0.010 1.000 1 2019 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.763 0.160 7 55181312 missense variant G/T snv 0.010 1.000 1 2016 2016
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.763 0.160 7 55181312 missense variant G/T snv 0.010 1.000 1 2017 2017