Disease | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||||
---|---|---|---|---|---|---|---|---|---|---|---|
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Prevalence and functional consequence of TP53 mutations in pediatric adrenocortical carcinoma: a children's oncology group study. | 25584008 | 2015 | |||||
Li-Fraumeni Syndrome
|
0.800 | GeneticVariation | UNIPROT | American Society of Clinical Oncology Expert Statement: collection and use of a cancer family history for oncology providers. | 24493721 | 2014 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Two hot spot mutant p53 mouse models display differential gain of function in tumorigenesis. | 23538418 | 2013 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Dominant-negative features of mutant TP53 in germline carriers have limited impact on cancer outcomes. | 21343334 | 2011 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study. | 21601526 | 2011 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome. | 21305319 | 2011 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Analysis of the DNA-binding activity of p53 mutants using functional protein microarrays and its relationship to transcriptional activation. | 20128691 | 2010 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Transcriptional functionality of germ line p53 mutants influences cancer phenotype. | 17606709 | 2007 | |||||
Li-Fraumeni Syndrome
|
0.800 | GeneticVariation | UNIPROT | American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography. | 17392385 | 2007 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Identification of novel TP53 mutations in familial and sporadic cancer cases of German and Swiss origin. | 15381368 | 2004 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Germ-line mutations of TP53 in Li-Fraumeni families: an extended study of 39 families. | 9242456 | 1997 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Germ-line p53 mutations in 15 families with Li-Fraumeni syndrome. | 7887414 | 1995 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | p53 mosaicism with an exon 8 germline mutation in the founder of a cancer-prone pedigree. | 1359493 | 1992 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma. | 1565143 | 1992 | |||||
Li-Fraumeni Syndrome
|
0.800 | CausalMutation | CLINVAR | The p53 tumour suppressor gene. | 2046748 | 1991 | |||||
Li-Fraumeni Syndrome
|
0.800 | GeneticVariation | CLINVAR |