rs2298881, ERCC1

N. diseases: 25
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.
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.653 0.400 19 45423658 intron variant C/A;T snv 0.030 1.000 3 2011 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.653 0.400 19 45423658 intron variant C/A;T snv 0.030 0.667 3 2014 2017
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.653 0.400 19 45423658 intron variant C/A;T snv 0.030 1.000 3 2011 2014
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.653 0.400 19 45423658 intron variant C/A;T snv 0.030 1.000 3 2011 2014
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.653 0.400 19 45423658 intron variant C/A;T snv 0.020 1.000 2 2015 2015
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.653 0.400 19 45423658 intron variant C/A;T snv 0.020 1.000 2 2014 2015
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.653 0.400 19 45423658 intron variant C/A;T snv 0.020 1.000 2 2014 2015
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.653 0.400 19 45423658 intron variant C/A;T snv 0.020 1.000 2 2015 2019
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.653 0.400 19 45423658 intron variant C/A;T snv 0.020 1.000 2 2015 2015
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.653 0.400 19 45423658 intron variant C/A;T snv 0.020 1.000 2 2015 2015
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.653 0.400 19 45423658 intron variant C/A;T snv 0.020 1.000 2 2014 2015
Xeroderma pigmentosum, group F
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
31 0.653 0.400 19 45423658 intron variant C/A;T snv 0.020 1.000 2 2014 2014
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2014 2014
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2018 2018
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2018 2018
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2017 2017
Glioma
CUI: C0017638
Disease: Glioma
353 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2014 2014
High grade glioma
CUI: C4722099
Disease: High grade glioma
15 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2014 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2016 2016
Malignant Glioma
CUI: C0555198
Disease: Malignant Glioma
22 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2014 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2014 2014
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2012 2012
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2018 2018
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.653 0.400 19 45423658 intron variant C/A;T snv 0.010 1.000 1 2012 2012