rs1131691003, TP53

N. diseases: 12
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.
ADRENOCORTICAL CARCINOMA, HEREDITARY
7 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
BASAL CELL CARCINOMA, SUSCEPTIBILITY TO, 7
7 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
Choroid Plexus Papilloma
CUI: C0205770
Disease: Choroid Plexus Papilloma
17 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
GLIOMA SUSCEPTIBILITY 1
CUI: C2750850
Disease: GLIOMA SUSCEPTIBILITY 1
14 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
LI-FRAUMENI SYNDROME 1
CUI: C1835398
Disease: LI-FRAUMENI SYNDROME 1
39 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.752 0.360 17 7676381 splice donor variant C/A;G snv 0.700 0