Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12947788
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs12947788
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10
CUI: C0812413
Disease: Malignant Pleural Mesothelioma
Malignant Pleural Mesothelioma 		0.010 1.000 1 2013 2013
dbSNP: rs12947788
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
Hereditary Nonpolyposis Colorectal Cancer 		0.010 1.000 1 2016 2016
dbSNP: rs12947788
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10
CUI: C4552100
Disease: Lynch Syndrome
Lynch Syndrome 		0.010 1.000 1 2016 2016
dbSNP: rs12947788
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10
CUI: C0853879
Disease: Invasive carcinoma of breast
Invasive carcinoma of breast 		0.010 1.000 1 2007 2007
dbSNP: rs12947788
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs12947788
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas 		0.010 1.000 1 2015 2015
dbSNP: rs12947788
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2013 2013