rs1057519977, TP53

N. diseases: 13
Source: CLINVAR ×
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.
Squamous cell carcinoma of the head and neck
179 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
135 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
66 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6385 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 1999 1999
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
76 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
314 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
141 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
216 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
118 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
96 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
114 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
211 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016