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.
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
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 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
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
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
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
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
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
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
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
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
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
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