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.
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
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
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2009 2009
Metastasis from malignant tumor of prostate
CUI: C1282496
Disease: Metastasis from malignant tumor of prostate
18 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2011 2011
Metastatic Prostate Carcinoma
CUI: C0936223
Disease: Metastatic Prostate Carcinoma
24 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2011 2011
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.710 1.000 1 2005 2005
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2005 2005
Primary Myelofibrosis
CUI: C0001815
Disease: Primary Myelofibrosis
29 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2012 2012
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2007 2007
Squamous cell carcinoma of pharynx
CUI: C1319317
Disease: Squamous cell carcinoma of pharynx
4 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2011 2011
Tumor Progression
CUI: C0178874
Disease: Tumor Progression
72 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2018 2018
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
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
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
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
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
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 0
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 0
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 0
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 0.700 0