rs28934578, TP53

N. diseases: 47
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.
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2019 2019
Adrenocortical carcinoma
CUI: C0206686
Disease: Adrenocortical carcinoma
46 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2006 2006
ADRENOCORTICAL CARCINOMA, HEREDITARY
CUI: C1859972
Disease: ADRENOCORTICAL CARCINOMA, HEREDITARY
7 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 0
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2011 2011
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2017 2017
BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7
CUI: C3553606
Disease: BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7
7 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 0
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.060 1.000 6 2009 2018
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.030 1.000 3 2011 2017
Carcinoma, Neuroendocrine
CUI: C0206695
Disease: Carcinoma, Neuroendocrine
7 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2017 2017
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2011 2011
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2017 2017
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2005 2005
Choroid Plexus Papilloma
CUI: C0205770
Disease: Choroid Plexus Papilloma
17 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 0
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 0
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2009 2009
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2011 2011
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2011 2011
GLIOMA SUSCEPTIBILITY 1
CUI: C2750850
Disease: GLIOMA SUSCEPTIBILITY 1
14 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 0
Large cell neuroendocrine carcinoma
CUI: C1265996
Disease: Large cell neuroendocrine carcinoma
3 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2017 2017
Leukoencephalopathy, Progressive Multifocal
CUI: C0023524
Disease: Leukoencephalopathy, Progressive Multifocal
4 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2013 2013
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
206 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.820 1.000 28 1990 2017
LI-FRAUMENI SYNDROME 1
CUI: C1835398
Disease: LI-FRAUMENI SYNDROME 1
39 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 1.000 14 1997 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.710 1 2017 2017
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2017 2017