rs2227983, EGFR

N. diseases: 31
Source: BEFREE ×
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
601 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.050 1.000 5 2007 2011
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2145 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.040 1.000 4 2012 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
2154 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.040 1.000 4 2012 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.030 1.000 3 2007 2018
Diarrhea
CUI: C0011991
Disease: Diarrhea
50 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.020 0.500 2 2010 2010
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.020 1.000 2 2007 2019
Skin toxicity
CUI: C1167791
Disease: Skin toxicity
24 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.020 1.000 2 2010 2016
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
171 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.020 1.000 2 2012 2016
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2008 2008
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
97 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2008 2008
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
167 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2009 2009
Advanced lung cancer
CUI: C4524268
Disease: Advanced lung cancer
9 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2009 2009
Bronchitis
CUI: C0006277
Disease: Bronchitis
4 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2013 2013
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
200 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2009 2009
cervical cancer
CUI: C4048328
Disease: cervical cancer
257 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2019 2019
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
266 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2019 2019
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2011 2011
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2009 2009
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2019 2019
Metastatic Colorectal Carcinoma
CUI: C4744564
Disease: Metastatic Colorectal Carcinoma
7 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2007 2007
Neoplasms
CUI: C0027651
Disease: Neoplasms
1571 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2014 2014
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
110 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2005 2005
Recurrent tumor
CUI: C0521158
Disease: Recurrent tumor
33 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2007 2007
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
676 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2017 2017
Secondary malignant neoplasm of colon and/or rectum
CUI: C4721579
Disease: Secondary malignant neoplasm of colon and/or rectum
40 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2014 2014