Source: BEFREE

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: rs909797662
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.080 0.875 8 2010 2019
dbSNP: rs909797662
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
Secondary malignant neoplasm of colon and/or rectum 		0.050 0.800 5 2010 2016
dbSNP: rs909797662
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.040 1.000 4 2016 2019
dbSNP: rs909797662
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		0.030 1.000 3 2015 2018
dbSNP: rs909797662
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.030 1.000 3 2015 2018
dbSNP: rs909797662
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv
CUI: C4688318
Disease: Refractory Colorectal Carcinoma
Refractory Colorectal Carcinoma 		0.010 1.000 1 2010 2010
dbSNP: rs909797662
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2016 2016
dbSNP: rs909797662
rs909797662
EGFR
0.790 0.120 7 55191837 missense variant G/A snv
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2016 2016