TP53, tumor protein p53, 7157

N. diseases: 2494; N. variants: 527
Disease: Familial (FPAH) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912664
rs121912664
Entrez Id: 7157
Gene Symbol: TP53
TP53
CUI: C1611743
Disease:
Familial (FPAH) 		0.010 GeneticVariation BEFREE A TP53 germline mutation, R337H, has been previously described in children from southern Brazil with adrenocortical tumours but no documented familial history of other cancers. 16494995 2007