{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":4,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:20001","source":"HGNC:20001|proprotein convertase subtilisin/kexin type 9","targets":["1015123|NM_174936.4(PCSK9):c.653G>C (p.Arg218Thr)|single nucleotide variant|Likely pathogenic|PCSK9|criteria provided, single submitter|1","1120257|NM_174936.4(PCSK9):c.1906A>C (p.Ser636Arg)|single nucleotide variant|Likely pathogenic|PCSK9|criteria provided, single submitter|1","4277664|NM_174936.4(PCSK9):c.399+1G>A|single nucleotide variant|Likely pathogenic|PCSK9|criteria provided, single submitter|1","438337|NM_174936.4(PCSK9):c.1061A>T (p.Asn354Ile)|single nucleotide variant|Likely pathogenic|PCSK9|criteria provided, single submitter|1"]}]}