rs28934576, TP53

N. diseases: 64
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.
LI-FRAUMENI SYNDROME 1
CUI: C1835398
Disease: LI-FRAUMENI SYNDROME 1
61 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.800 23 1990 2017
Li-Fraumeni-Like Syndrome
CUI: C2675080
Disease: Li-Fraumeni-Like Syndrome
55 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.700 8 1990 2010
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
87 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.720 1.000 15 1992 2017
Anaplastic thyroid carcinoma
CUI: C0238461
Disease: Anaplastic thyroid carcinoma
3 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.700 2 1992 1993
Adult T-Cell Lymphoma/Leukemia
CUI: C0023493
Disease: Adult T-Cell Lymphoma/Leukemia
5 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 1992 1992
Leukemia, T-Cell
CUI: C0023492
Disease: Leukemia, T-Cell
4 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 1992 1992
Anaplastic carcinoma
CUI: C0205696
Disease: Anaplastic carcinoma
3 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 1993 1993
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
735 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1 1993 1993
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
409 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1 1993 1993
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
400 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1 1993 1993
Undifferentiated carcinoma
CUI: C0205698
Disease: Undifferentiated carcinoma
2 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 1993 1993
Xeroderma Pigmentosum, Complementation Group D
39 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1 1995 1995
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
303 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.700 3 1998 2016
Adenoma
CUI: C0001430
Disease: Adenoma
73 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 1999 1999
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
4866 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.700 9 2000 2018
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
165 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 2001 2001
Ataxia Telangiectasia
CUI: C0004135
Disease: Ataxia Telangiectasia
403 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.020 1.000 2 2005 2009
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
159 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 2005 2005
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
74 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.720 1.000 3 2007 2015
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
61 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.020 1.000 2 2007 2012
Skin Neoplasms
CUI: C0037286
Disease: Skin Neoplasms
4 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 2007 2007
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
129 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.020 1.000 2 2008 2018
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
145 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 2008 2008
Glioma
CUI: C0017638
Disease: Glioma
180 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 2008 2008
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
106 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 2008 2008