rs878854066, TP53

N. diseases: 213
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.
Undifferentiated carcinoma
CUI: C0205698
Disease: Undifferentiated carcinoma
8 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2003 2003
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.050 0.800 5 2004 2017
Sporadic Breast Carcinoma
CUI: C1336076
Disease: Sporadic Breast Carcinoma
46 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2004 2012
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2004 2004
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2004 2004
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2004 2004
Oestrogen receptor positive breast cancer
CUI: C2938924
Disease: Oestrogen receptor positive breast cancer
58 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2004 2004
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.100 0.909 33 2005 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.100 0.857 14 2005 2017
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.080 0.750 8 2005 2014
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.080 0.750 8 2005 2014
Glaucoma
CUI: C0017601
Disease: Glaucoma
198 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.040 0.500 4 2005 2018
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2005 2009
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2005 2008
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2005 2005
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2005 2009
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
59 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2005 2005
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.100 0.750 20 2006 2018
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.100 0.933 15 2006 2018
melanoma
CUI: C0025202
Disease: melanoma
515 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.100 0.900 10 2006 2017
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.070 1.000 7 2006 2018
Malignant neoplasm of skin
CUI: C0007114
Disease: Malignant neoplasm of skin
38 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.040 1.000 4 2006 2013
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2006 2006
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2006 2009
Experimental Organism Basal Cell Carcinoma
CUI: C3811653
Disease: Experimental Organism Basal Cell Carcinoma
63 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2006 2009