rs1042522, TP53

N. diseases: 242
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.
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.020 1.000 2 2005 2009
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.020 1.000 2 2005 2008
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.833 48 2003 2020
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.080 1.000 8 2008 2016
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.030 1.000 3 2010 2015
Carcinoma in situ of uterine cervix
CUI: C0851140
Disease: Carcinoma in situ of uterine cervix
18 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1.000 1 2009 2009
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.080 1.000 8 2010 2015
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1.000 1 2009 2009
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.850 20 2000 2018
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.020 1.000 2 2006 2009
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.040 1.000 4 2012 2015
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.030 1.000 3 2017 2019
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.030 1.000 3 2011 2019
cervical cancer
CUI: C4048328
Disease: cervical cancer
268 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.923 13 2002 2018
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.020 1.000 2 2014 2014
Cervical Squamous Cell Carcinoma
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
44 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1.000 1 2000 2000
Cervix carcinoma
CUI: C0302592
Disease: Cervix carcinoma
283 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.929 14 2002 2018
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.020 1.000 2 2009 2013
Childhood Acute Megakaryoblastic Leukemia
CUI: C0279650
Disease: Childhood Acute Megakaryoblastic Leukemia
4 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1.000 1 2000 2000
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1.000 1 2013 2013
Childhood Hodgkin Lymphoma
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
29 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1 2011 2011
Childhood Kidney Wilms Tumor
CUI: C1333015
Disease: Childhood Kidney Wilms Tumor
36 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.020 1.000 2 2017 2019
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.020 2 2012 2016
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1.000 1 2012 2012
Childhood Medulloblastoma
CUI: C0278510
Disease: Childhood Medulloblastoma
25 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.020 1.000 2 2003 2012