rs28934874, TP53

N. diseases: 21
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.
Li-Fraumeni Syndrome
CUI: C0085390
Disease: Li-Fraumeni Syndrome
206 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.800 1.000 19 1990 2014
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.710 1.000 2 2014 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 11 1991 2018
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Adenoid Cystic Carcinoma
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
30 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Serous cystadenocarcinoma ovary
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
99 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
348 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
158 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Uterine Carcinosarcoma
CUI: C0280630
Disease: Uterine Carcinosarcoma
80 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Breast adenocarcinoma
CUI: C0858252
Disease: Breast adenocarcinoma
7 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 0
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.695 0.480 17 7675161 missense variant G/A;C;T snv 0.700 0