rs909797662, EGFR

N. diseases: 8
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.
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.790 0.120 7 55191837 missense variant G/A snv 0.080 0.875 8 2010 2019
Secondary malignant neoplasm of colon and/or rectum
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
68 0.790 0.120 7 55191837 missense variant G/A snv 0.050 0.800 5 2010 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.120 7 55191837 missense variant G/A snv 0.040 1.000 4 2016 2019
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.790 0.120 7 55191837 missense variant G/A snv 0.030 1.000 3 2015 2018
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.790 0.120 7 55191837 missense variant G/A snv 0.030 1.000 3 2015 2018
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.790 0.120 7 55191837 missense variant G/A snv 0.010 1.000 1 2016 2016
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.790 0.120 7 55191837 missense variant G/A snv 0.010 1.000 1 2016 2016
Refractory Colorectal Carcinoma
CUI: C4688318
Disease: Refractory Colorectal Carcinoma
2 0.790 0.120 7 55191837 missense variant G/A snv 0.010 1.000 1 2010 2010