rs1057520001, TP53

N. diseases: 23
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 0.677 0.360 17 7674886 missense variant A/C;G snv 0.030 1.000 3 1997 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.677 0.360 17 7674886 missense variant A/C;G snv 0.020 1.000 2 2010 2019
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2004 2004
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2007 2007
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2004 2004
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1 2007 2007
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2004 2004
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2012 2012
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2004 2004
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2004 2004
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2004 2004
Malignant neoplasm of kidney
CUI: C0740457
Disease: Malignant neoplasm of kidney
22 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2007 2007
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2007 2007
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2019 2019
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 1995 1995
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 1995 1995
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2019 2019
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2007 2007
Renal carcinoma
CUI: C1378703
Disease: Renal carcinoma
21 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2007 2007
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1 2007 2007
Skin toxicity
CUI: C1167791
Disease: Skin toxicity
24 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2006 2006
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2007 2007
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.677 0.360 17 7674886 missense variant A/C;G snv 0.010 1.000 1 2007 2007