rs1057519848, EGFR

N. diseases: 72
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.
newly diagnosed non-small cell lung cancer
3 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.010 1.000 1 2018 2018
Papillary adenocarcinoma
CUI: C0001420
Disease: Papillary adenocarcinoma
3 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.010 1.000 1 2018 2018
Primary Lesion
CUI: C1402294
Disease: Primary Lesion
8 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.010 1.000 1 2018 2018
Signs and Symptoms, Respiratory
CUI: C0037090
Disease: Signs and Symptoms, Respiratory
10 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.010 1.000 1 2018 2018
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.100 0.933 60 2009 2019
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.100 0.975 40 2005 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.100 0.968 31 2006 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.100 0.968 31 2006 2019
Metastatic non-small cell lung cancer
11 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.100 1.000 12 2013 2019
Lung Neoplasms
CUI: C0024121
Disease: Lung Neoplasms
39 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.060 1.000 6 2012 2019
Adenocarcinoma of lung, stage IV
CUI: C0854988
Disease: Adenocarcinoma of lung, stage IV
6 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.040 1.000 4 2013 2019
Progressive cGVHD
CUI: C3539781
Disease: Progressive cGVHD
40 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.040 1.000 4 2011 2019
Progressive Neoplastic Disease
CUI: C0677932
Disease: Progressive Neoplastic Disease
40 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.040 1.000 4 2011 2019
Metastatic Malignant Neoplasm to the Leptomeninges
9 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.030 1.000 3 2009 2019
CNS metastases
CUI: C0686377
Disease: CNS metastases
14 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.010 1.000 1 2019 2019
HER2 gene amplification
CUI: C1512127
Disease: HER2 gene amplification
14 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.010 1.000 1 2019 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.010 1.000 1 2019 2019
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.010 1.000 1 2019 2019
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.800 0.983 176 2004 2020
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.100 1.000 58 2005 2020
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.100 0.941 34 2005 2020
Hyperplastic Polyp
CUI: C0333983
Disease: Hyperplastic Polyp
22 0.570 0.560 7 55191822 missense variant TG/GT mnv 0.010 1.000 1 2020 2020