rs28929495, EGFR

N. diseases: 9
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 0.807 0.120 7 55174014 missense variant G/A;C;T snv 0.750 1.000 21 2004 2019
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.807 0.120 7 55174014 missense variant G/A;C;T snv 0.720 1.000 3 2016 2018
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.807 0.120 7 55174014 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.807 0.120 7 55174014 missense variant G/A;C;T snv 0.020 1.000 2 2007 2018
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.807 0.120 7 55174014 missense variant G/A;C;T snv 0.010 1.000 1 2016 2016
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.807 0.120 7 55174014 missense variant G/A;C;T snv 0.010 1.000 1 2014 2014
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.807 0.120 7 55174014 missense variant G/A;C;T snv 0.010 1.000 1 2014 2014
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.807 0.120 7 55174014 missense variant G/A;C;T snv 0.010 1.000 1 2017 2017
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.807 0.120 7 55174014 missense variant G/A;C;T snv 0.010 1.000 1 2013 2013