rs397517132, EGFR

N. diseases: 48
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.
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.623 0.280 7 55191846 missense variant A/T snv 0.060 1.000 6 2006 2018
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.623 0.280 7 55191846 missense variant A/T snv 0.050 1.000 5 2006 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.623 0.280 7 55191846 missense variant A/T snv 0.050 1.000 5 2006 2018
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.623 0.280 7 55191846 missense variant A/T snv 0.050 1.000 5 2006 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.623 0.280 7 55191846 missense variant A/T snv 0.100 0.913 23 2008 2019
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.623 0.280 7 55191846 missense variant A/T snv 0.060 1.000 6 2008 2016
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.623 0.280 7 55191846 missense variant A/T snv 0.020 1.000 2 2008 2016
Malignant neoplasm of colon and/or rectum
502 0.623 0.280 7 55191846 missense variant A/T snv 0.100 1.000 13 2010 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.623 0.280 7 55191846 missense variant A/T snv 0.100 0.967 30 2011 2019
melanoma
CUI: C0025202
Disease: melanoma
515 0.623 0.280 7 55191846 missense variant A/T snv 0.100 0.941 17 2011 2019
Secondary malignant neoplasm of colon and/or rectum
68 0.623 0.280 7 55191846 missense variant A/T snv 0.100 1.000 14 2011 2019
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.623 0.280 7 55191846 missense variant A/T snv 0.100 1.000 13 2011 2019
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.623 0.280 7 55191846 missense variant A/T snv 0.090 1.000 9 2011 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.623 0.280 7 55191846 missense variant A/T snv 0.070 1.000 7 2011 2019
Marinesco-Sjogren syndrome
CUI: C0024814
Disease: Marinesco-Sjogren syndrome
8 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2011 2011
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.623 0.280 7 55191846 missense variant A/T snv 0.100 1.000 11 2012 2018
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.623 0.280 7 55191846 missense variant A/T snv 0.060 1.000 6 2012 2015
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
45 0.623 0.280 7 55191846 missense variant A/T snv 0.020 1.000 2 2012 2014
Acute Promyelocytic Leukemia
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
21 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2012 2012
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2012 2012
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2012 2012
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.623 0.280 7 55191846 missense variant A/T snv 0.040 0.750 4 2013 2017
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.623 0.280 7 55191846 missense variant A/T snv 0.030 0.667 3 2013 2014
Anaplastic thyroid carcinoma
CUI: C0238461
Disease: Anaplastic thyroid carcinoma
16 0.623 0.280 7 55191846 missense variant A/T snv 0.020 1.000 2 2013 2016
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.623 0.280 7 55191846 missense variant A/T snv 0.020 0.500 2 2013 2017