Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1064795203
rs1064795203
TP53
C 0.700 GeneticVariation CLINVAR Mutational processes shape the landscape of TP53 mutations in human cancer. 30224644

2018
dbSNP: rs1064795203
rs1064795203
TP53
C 0.700 GeneticVariation CLINVAR The frequency of cancer predisposition gene mutations in hereditary breast and ovarian cancer patients in Taiwan: From BRCA1/2 to multi-gene panels. 28961279

2017
dbSNP: rs1064795203
rs1064795203
TP53
C 0.700 GeneticVariation CLINVAR Detection of novel germline mutations for breast cancer in non-BRCA1/2 families. 26094658

2015
dbSNP: rs1064795203
rs1064795203
TP53
C 0.700 GeneticVariation CLINVAR Multiple malignancies in a child with de novo TP53 mutation. 21345075

2011
dbSNP: rs1064795203
rs1064795203
TP53
C 0.700 GeneticVariation CLINVAR Functional assessment of p53 in chronic lymphocytic leukemia. 22829111

2011
dbSNP: rs1064795203
rs1064795203
TP53
C 0.700 GeneticVariation CLINVAR Understanding the function-structure and function-mutation relationships of p53 tumor suppressor protein by high-resolution missense mutation analysis. 12826609

2003