rs11540652, TP53

N. diseases: 57
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.
GLIOMA SUSCEPTIBILITY 1
CUI: C2750850
Disease: GLIOMA SUSCEPTIBILITY 1
14 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Malignant neoplasm of large intestine
375 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0
Sarcoma
CUI: C1261473
Disease: Sarcoma
42 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 0.700 0