rs1042522, TP53

N. diseases: 242
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.
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.833 48 2003 2020
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.833 48 2003 2020
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.933 45 2002 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.921 38 2005 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.971 34 2003 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.727 22 2006 2019
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.850 20 2000 2018
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.850 20 2000 2018
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.850 20 2000 2018
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.867 15 2005 2017
Malignant neoplasm of colon and/or rectum
502 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.867 15 2006 2018
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.929 14 2002 2018
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.923 13 2002 2018
Malignant tumor of cervix
CUI: C0007847
Disease: Malignant tumor of cervix
245 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.923 13 2002 2018
melanoma
CUI: C0025202
Disease: melanoma
515 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.833 12 2006 2019
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.909 11 2009 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.900 10 2009 2015
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.090 0.889 9 2009 2015
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.090 0.889 9 1999 2018
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.080 1.000 8 2010 2015
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.080 1.000 8 2008 2016
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.080 1.000 8 2010 2015
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.080 0.750 8 2005 2014
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.080 0.875 8 2009 2015
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.080 0.875 8 2009 2015