Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057517840
rs1057517840
TP53
CUI: C0085390
Disease: Li-Fraumeni Syndrome
Li-Fraumeni Syndrome 		T 0.700 CausalMutation CLINVAR The p53 gene in pediatric therapy-related leukemia and myelodysplasia. 8639798

1996