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.
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2013 2013
Childhood Hodgkin Lymphoma
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
29 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1 2011 2011
Childhood Kidney Wilms Tumor
CUI: C1333015
Disease: Childhood Kidney Wilms Tumor
36 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2017 2017
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2012 2012
Childhood Myelodysplastic Syndrome
CUI: C2347761
Disease: Childhood Myelodysplastic Syndrome
20 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2012 2012
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2019 2019
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
Childhood Oligodendroglioma
CUI: C0280475
Disease: Childhood Oligodendroglioma
19 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2013 2013
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2006 2006
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2013 2013
Cutaneous lymphoma
CUI: C1276146
Disease: Cutaneous lymphoma
3 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1 2006 2006
Cutaneous Mastocytosis
CUI: C1136033
Disease: Cutaneous Mastocytosis
18 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2016 2016
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1 2017 2017
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2013 2013
Drug usage
CUI: C0242510
Disease: Drug usage
21 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2007 2007
Epithelioid angiomyolipoma
CUI: C4518194
Disease: Epithelioid angiomyolipoma
3 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2015 2015
Extrapulmonary Small Cell Carcinoma
CUI: C4722419
Disease: Extrapulmonary Small Cell Carcinoma
11 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2014 2014
Familial Retinoblastoma
CUI: C0751483
Disease: Familial Retinoblastoma
4 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2011 2011
Febrile Neutropenia
CUI: C0746883
Disease: Febrile Neutropenia
14 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1 2012 2012
Fibroid Tumor
CUI: C0023267
Disease: Fibroid Tumor
14 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2019 2019
Gastric Cardia Adenocarcinoma
CUI: C1333762
Disease: Gastric Cardia Adenocarcinoma
11 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2007 2007
Gastric Cardia Carcinoma
CUI: C1333763
Disease: Gastric Cardia Carcinoma
13 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2007 2007
Gastroesophageal reflux disease
CUI: C0017168
Disease: Gastroesophageal reflux disease
52 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2013 2013
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2007 2007
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.010 1.000 1 2013 2013