Germline Genetic Variants in Cancer-Susceptibility Genes in Patients with Osteosarcoma

We conducted whole-exome sequencing of germline DNA from patients with osteosarcoma to estimate the frequency of pathogenic/likely pathogenic germline genetic variants in known cancer-susceptibility genes in a large population of osteosarcoma patients unselected for family history.

• Type: Case Set
• Archiver: The database of Genotypes and Phenotypes (dbGaP)