rs121912651, TP53

N. diseases: 21
Source: BEFREE ×
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.
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
37 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.820 1.000 2 1990 2015
Neoplasms
CUI: C0027651
Disease: Neoplasms
1571 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.760 0.857 6 1999 2019
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
183 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.710 1.000 1 2016 2017
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
247 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.710 1.000 1 2010 2016
Small cell carcinoma of lung
CUI: C0149925
Disease: Small cell carcinoma of lung
61 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.710 1.000 1 1991 2016
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.030 0.667 3 2007 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.030 0.667 3 2007 2019
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
238 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.020 1.000 2 2004 2008
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
236 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.020 1.000 2 2004 2008
Anaplastic thyroid carcinoma
CUI: C0238461
Disease: Anaplastic thyroid carcinoma
16 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2005 2005
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2007 2007
Carcinoma
CUI: C0007097
Disease: Carcinoma
90 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2008 2008
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2008 2008
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2008 2008
Chronic graft-versus-host disease
CUI: C0867389
Disease: Chronic graft-versus-host disease
17 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2018 2018
Lichen Sclerosus et Atrophicus
CUI: C0023652
Disease: Lichen Sclerosus et Atrophicus
2 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2007 2007
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
163 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1 2015 2015
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2013 2013
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
234 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2008 2008
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
320 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2018 2018
Tumors of Adrenal Cortex
CUI: C0001618
Disease: Tumors of Adrenal Cortex
5 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2008 2008