rs587780071, TP53

N. diseases: 11
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 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
114 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
118 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
216 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
115 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
142 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
Mammary Neoplasms
CUI: C1458155
Disease: Mammary Neoplasms
314 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
Serous cystadenocarcinoma ovary
CUI: C0279663
Disease: Serous cystadenocarcinoma ovary
99 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of the head and neck
179 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
141 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
69 0.732 0.240 17 7674951 missense variant G/A snv 0.700 1.000 1 2016 2016