Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131691026
rs1131691026
TP53
T 0.700 CausalMutation CLINVAR TP53 Variations in Human Cancers: New Lessons from the IARC TP53 Database and Genomics Data. 27328919

2016
dbSNP: rs1131691026
rs1131691026
TP53
T 0.700 CausalMutation CLINVAR Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study. 27501770

2016
dbSNP: rs1131691026
rs1131691026
TP53
T 0.700 CausalMutation CLINVAR Anaplastic rhabdomyosarcoma in TP53 germline mutation carriers. 24382691

2014
dbSNP: rs1131691026
rs1131691026
TP53
T 0.700 CausalMutation CLINVAR Early onset HER2-positive breast cancer is associated with germline TP53 mutations. 21761402

2012
dbSNP: rs1131691026
rs1131691026
TP53
T 0.700 CausalMutation CLINVAR Heterozygous TP53stop146/R72P fibroblasts from a Li-Fraumeni syndrome patient with impaired response to DNA damage. 20198344

2010