rs12947788, TP53

N. diseases: 8
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.280 17 7674109 intron variant G/A snv 0.10 0.010 1.000 1 2016 2016
Hereditary Nonpolyposis Colorectal Cancer
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
1331 0.776 0.280 17 7674109 intron variant G/A snv 0.10 0.010 1.000 1 2016 2016
Invasive carcinoma of breast
CUI: C0853879
Disease: Invasive carcinoma of breast
21 0.776 0.280 17 7674109 intron variant G/A snv 0.10 0.010 1.000 1 2007 2007
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.776 0.280 17 7674109 intron variant G/A snv 0.10 0.010 1.000 1 2016 2016
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.776 0.280 17 7674109 intron variant G/A snv 0.10 0.010 1.000 1 2015 2015
Malignant Pleural Mesothelioma
CUI: C0812413
Disease: Malignant Pleural Mesothelioma
15 0.776 0.280 17 7674109 intron variant G/A snv 0.10 0.010 1.000 1 2013 2013
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.776 0.280 17 7674109 intron variant G/A snv 0.10 0.010 1.000 1 2013 2013
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.776 0.280 17 7674109 intron variant G/A snv 0.10 0.010 1.000 1 2015 2015