rs121912666, TP53

N. diseases: 34
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.
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2014 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.710 1.000 2 2016 2019
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.710 1.000 2 2007 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.700 1.000 3 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.030 1.000 3 2010 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.030 1.000 3 2010 2019
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.700 1.000 4 2010 2014
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.040 1.000 4 2005 2017
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
206 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 0.820 1.000 43 1990 2018