rs2227983, EGFR

N. diseases: 31
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.
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
139 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
168 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
243 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
268 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
283 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
1644 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
112 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
2387 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
68 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2014 2014
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2014 2014
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2009 2009
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2009 2009
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2007 2007
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1 2010 2010
Xeroderma Pigmentosum, Complementation Group D
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
111 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 0.010 1.000 1 2011 2011
Diarrhea
CUI: C0011991
Disease: Diarrhea
63 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