rs755174338, ERCC2

N. diseases: 15
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.
Squamous cell carcinoma of the head and neck
348 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.020 1.000 2 2011 2012
Adult Myelodysplastic Syndrome
CUI: C3900098
Disease: Adult Myelodysplastic Syndrome
20 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2016 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2005 2005
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2007 2007
Childhood Myelodysplastic Syndrome
CUI: C2347761
Disease: Childhood Myelodysplastic Syndrome
20 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2016 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2005 2005
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2007 2007
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2012 2012
MYELODYSPLASTIC SYNDROME
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
95 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2016 2016
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2014 2014
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2006 2006
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2012 2012
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2007 2007
Xeroderma Pigmentosum, Complementation Group D
111 0.732 0.360 19 45364096 missense variant C/T snv 2.6E-05 1.4E-05 0.010 1.000 1 2016 2016