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.
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
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
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2013 2013
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2013 2013
Malignant neoplasm of colon stage IV
CUI: C0278484
Disease: Malignant neoplasm of colon stage IV
7 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2013 2013
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
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
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2014 2014
Secondary Neoplasm
CUI: C2939419
Disease: Secondary Neoplasm
85 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1 2014 2014
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
BRONCHIAL ADENOCARCINOMA
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
1 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2015 2015
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2015 2015
Glioma
CUI: C0017638
Disease: Glioma
353 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2015 2015
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
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
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
Carcinomatosis of peritoneal cavity
CUI: C0346990
Disease: Carcinomatosis of peritoneal cavity
3 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2016 2016
Epithelioid glioblastoma
CUI: C4289580
Disease: Epithelioid glioblastoma
3 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2016 2016
Gastro-enteropancreatic neuroendocrine tumor
CUI: C2930967
Disease: Gastro-enteropancreatic neuroendocrine tumor
4 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2016 2016
Monosomy
CUI: C0026499
Disease: Monosomy
11 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2016 2016
Neuroendocrine Tumors
CUI: C0206754
Disease: Neuroendocrine Tumors
20 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2016 2016
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
Ameloblastoma
CUI: C0002448
Disease: Ameloblastoma
4 0.623 0.280 7 55191846 missense variant A/T snv 0.030 1.000 3 2014 2017