rs1057519987, TP53

N. diseases: 10
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.
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.776 0.280 17 7673810 missense variant A/C snv 0.700 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.776 0.280 17 7673810 missense variant A/C snv 0.700 1.000 1 2016 2016
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.776 0.280 17 7673810 missense variant A/C snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.776 0.280 17 7673810 missense variant A/C snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
385 0.776 0.280 17 7673810 missense variant A/C snv 0.700 1.000 1 2016 2016
Serous cystadenocarcinoma ovary
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
99 0.776 0.280 17 7673810 missense variant A/C snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of lung
CUI: C0149782
Disease: Squamous cell carcinoma of lung
283 0.776 0.280 17 7673810 missense variant A/C snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
92 0.776 0.280 17 7673810 missense variant A/C snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.776 0.280 17 7673810 missense variant A/C snv 0.700 1.000 1 2016 2016
Holt-Oram syndrome
CUI: C0265264
Disease: Holt-Oram syndrome
69 0.776 0.280 17 7673810 missense variant A/C snv 0.010 1.000 1 2006 2006