rs28934571, TP53

N. diseases: 31
Disease: Congenital absence of liver ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital absence of liver
CUI: C0266258
Disease: Congenital absence of liver
0.010 GeneticVariation BEFREE Aflatoxin-induced TP53 R249S mutation in hepatocellular carcinoma in Thailand: association with tumors developing in the absence of liver cirrhosis. 22675488 2012