Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555525703
rs1555525703
TP53
T 0.700 GeneticVariation CLINVAR Novel p53 splicing site mutation in Li-Fraumeni-like syndrome with osteosarcoma. 23409989

2013
dbSNP: rs1555525703
rs1555525703
TP53
T 0.700 GeneticVariation CLINVAR High frequency of de novo mutations in Li-Fraumeni syndrome. 19556618

2009
dbSNP: rs1555525703
rs1555525703
TP53
T 0.700 GeneticVariation CLINVAR The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families. 16494995

2007
dbSNP: rs1555525703
rs1555525703
TP53
T 0.700 GeneticVariation CLINVAR Novel p53 germline mutation in a patient with Li-Fraumeni syndrome. 14656244

2003