rs1057519988, TP53

N. diseases: 10
Source: INFERRED ×
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)
0.776 0.240 17 7673812 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
0.776 0.240 17 7673812 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
0.776 0.240 17 7673812 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
0.776 0.240 17 7673812 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
0.776 0.240 17 7673812 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Serous cystadenocarcinoma ovary
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
0.776 0.240 17 7673812 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
0.776 0.240 17 7673812 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
0.776 0.240 17 7673812 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
0.776 0.240 17 7673812 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
0.776 0.240 17 7673812 missense variant A/C;G;T snv 0.700 0