rs760101437, EGFR

N. diseases: 6
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.
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 0.030 1.000 3 2009 2015
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 0.020 1.000 2 2007 2010
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 0.010 1.000 1 2009 2009
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 0.010 1.000 1 2009 2009
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 0.010 1.000 1 2009 2009
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 0.010 1 2001 2001