rs863224683, TP53

N. diseases: 4
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.
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 17 7675224 missense variant G/A;C snv 0.010 1.000 1 2013 2013
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 17 7675224 missense variant G/A;C snv 0.010 1.000 1 2013 2013
Cervix Diseases
CUI: C0007867
Disease: Cervix Diseases
3 17 7675224 missense variant G/A;C snv 0.010 1.000 1 2017 2017
High-Grade Squamous Intraepithelial Lesions
CUI: C0333875
Disease: High-Grade Squamous Intraepithelial Lesions
8 17 7675224 missense variant G/A;C snv 0.010 1.000 1 2017 2017