{"context":{"query":">>mondo>>clinvar","source_dataset":"mondo","target_dataset":"clinvar"},"stats":{"queried":1,"total":2,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"MONDO:0002108","source":"MONDO:0002108|thyroid cancer","targets":["185440|NM_000051.4(ATM):c.7654C>A (p.His2552Asn)|single nucleotide variant|Uncertain significance|ATM|criteria provided, multiple submitters, no conflicts|11","186956|NM_000465.4(BARD1):c.632T>C (p.Leu211Ser)|single nucleotide variant|Uncertain significance|BARD1|criteria provided, multiple submitters, no conflicts|2"]}]}