{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":8,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:620","source":"HGNC:620|amyloid beta precursor protein","targets":["1298879|NM_000484.4(APP):c.2148C>G (p.Ile716Met)|single nucleotide variant|Likely pathogenic|APP|criteria provided, single submitter|21","1342870|NM_000484.4(APP):c.2155A>C (p.Thr719Pro)|single nucleotide variant|Likely pathogenic|APP|criteria provided, single submitter|21","18094|NM_000484.4(APP):c.2137G>A (p.Ala713Thr)|single nucleotide variant|Likely pathogenic|APP|criteria provided, multiple submitters, no conflicts|21","18103|NM_000484.4(APP):c.2113C>G (p.Leu705Val)|single nucleotide variant|Likely pathogenic|APP|criteria provided, single submitter|21","2628367|NM_000484.4(APP):c.2061A>C (p.Lys687Asn)|single nucleotide variant|Likely pathogenic|APP|criteria provided, single submitter|21","3382968|NM_000484.4(APP):c.2059A>C (p.Lys687Gln)|single nucleotide variant|Likely pathogenic|APP|criteria provided, single submitter|21","3690355|NM_000484.4(APP):c.2138C>A (p.Ala713Glu)|single nucleotide variant|Likely pathogenic|APP|criteria provided, single submitter|21","446855|NM_000484.4(APP):c.2032G>C (p.Asp678His)|single nucleotide variant|Likely pathogenic|APP|criteria provided, single submitter|21"]}]}