rs1131691029, TP53

N. diseases: 6
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.
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.827 0.160 17 7673794 missense variant C/G snv 0.700 1.000 3 2007 2010
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.827 0.160 17 7673794 missense variant C/G snv 0.700 0
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.827 0.160 17 7673794 missense variant C/G snv 0.010 1.000 1 2006 2006
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.827 0.160 17 7673794 missense variant C/G snv 0.010 1.000 1 2006 2006
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.827 0.160 17 7673794 missense variant C/G snv 0.010 1.000 1 2006 2006
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.827 0.160 17 7673794 missense variant C/G snv 0.010 1.000 1 2006 2006