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.
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.623 0.280 7 55191846 missense variant A/T snv 0.020 0.500 2 2013 2017
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
Ameloblastoma
CUI: C0002448
Disease: Ameloblastoma
4 0.623 0.280 7 55191846 missense variant A/T snv 0.030 1.000 3 2014 2017
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
Metastatic melanoma
CUI: C0278883
Disease: Metastatic melanoma
42 0.623 0.280 7 55191846 missense variant A/T snv 0.030 1.000 3 2015 2019
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
Childhood Pleomorphic Xanthoastrocytoma
CUI: C3899645
Disease: Childhood Pleomorphic Xanthoastrocytoma
7 0.623 0.280 7 55191846 missense variant A/T snv 0.020 1.000 2 2016 2019
Pleomorphic Xanthoastrocytoma
CUI: C0334586
Disease: Pleomorphic Xanthoastrocytoma
8 0.623 0.280 7 55191846 missense variant A/T snv 0.020 1.000 2 2016 2019
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
Pleural Effusion, Malignant
CUI: C0080032
Disease: Pleural Effusion, Malignant
6 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2017 2017
Cerebellar Neoplasms
CUI: C0007762
Disease: Cerebellar Neoplasms
5 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2018 2018
Advanced Melanoma
CUI: C4727838
Disease: Advanced Melanoma
5 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2019 2019
Malignant neoplasm of soft tissue
CUI: C4551686
Disease: Malignant neoplasm of soft tissue
32 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2019 2019
Sarcoma
CUI: C1261473
Disease: Sarcoma
42 0.623 0.280 7 55191846 missense variant A/T snv 0.010 1.000 1 2019 2019