rs28934571, TP53

N. diseases: 31
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.
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.645 0.360 17 7674216 missense variant C/A;G snv 0.800 1.000 22 1994 2020
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.645 0.360 17 7674216 missense variant C/A;G snv 0.700 0
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
206 0.645 0.360 17 7674216 missense variant C/A;G snv 0.700 0
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.645 0.360 17 7674216 missense variant C/A;G snv 0.700 0
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.645 0.360 17 7674216 missense variant C/A;G snv 0.100 1.000 11 1995 2020
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.645 0.360 17 7674216 missense variant C/A;G snv 0.050 1.000 5 2001 2013
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.645 0.360 17 7674216 missense variant C/A;G snv 0.030 1.000 3 2018 2019
Liver and Intrahepatic Biliary Tract Carcinoma
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
73 0.645 0.360 17 7674216 missense variant C/A;G snv 0.030 1.000 3 2018 2019
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.645 0.360 17 7674216 missense variant C/A;G snv 0.030 1.000 3 2018 2019
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.645 0.360 17 7674216 missense variant C/A;G snv 0.020 1.000 2 2012 2013
Hepatocarcinogenesis
CUI: C1512409
Disease: Hepatocarcinogenesis
24 0.645 0.360 17 7674216 missense variant C/A;G snv 0.020 1.000 2 2010 2013
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.645 0.360 17 7674216 missense variant C/A;G snv 0.020 1.000 2 2012 2013
Chronic liver disease
CUI: C0341439
Disease: Chronic liver disease
14 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2012 2012
Congenital absence of liver
CUI: C0266258
Disease: Congenital absence of liver
2 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2012 2012
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2015 2015
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
75 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1 2017 2017
gallbladder neoplasm
CUI: C0016978
Disease: gallbladder neoplasm
6 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2017 2017
Hepatoblastoma
CUI: C0206624
Disease: Hepatoblastoma
22 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2006 2006
Hepatocellular Adenoma
CUI: C0206669
Disease: Hepatocellular Adenoma
7 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2006 2006
HER2-negative breast cancer
CUI: C4733095
Disease: HER2-negative breast cancer
18 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2019 2019
HER2-positive carcinoma of breast
CUI: C1960398
Disease: HER2-positive carcinoma of breast
26 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2019 2019
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2013 2013
Liver neoplasms
CUI: C0023903
Disease: Liver neoplasms
7 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 1994 1994
Malignant neoplasm of gallbladder
CUI: C0153452
Disease: Malignant neoplasm of gallbladder
81 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1 2017 2017
Multiple adenomatous polyps
CUI: C0334294
Disease: Multiple adenomatous polyps
5 0.645 0.360 17 7674216 missense variant C/A;G snv 0.010 1.000 1 2006 2006