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.
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.030 0.667 3 2014 2015
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
Adult Medulloblastoma
CUI: C0278876
Disease: Adult Medulloblastoma
24 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2003 2012
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
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
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2012 2015
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2014 2014
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 2 2012 2016
Childhood Medulloblastoma
CUI: C0278510
Disease: Childhood Medulloblastoma
25 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2003 2012
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 0.500 2 2007 2009
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 0.500 2 2007 2019
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2010 2012
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 0.500 2 2007 2011
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 0.500 2 2014 2017
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2008 2011
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2015 2015
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
Gallbladder Carcinoma
CUI: C0235782
Disease: Gallbladder Carcinoma
75 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2007 2009
Hematologic Neoplasms
CUI: C0376545
Disease: Hematologic Neoplasms
60 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 0.500 2 2012 2015
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2012 2013
Hereditary Nonpolyposis Colorectal Cancer
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
1331 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 0.500 2 2006 2007
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
148 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 0.500 2 2011 2012
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
leukemia
CUI: C0023418
Disease: leukemia
144 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 2 2012 2016