{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":9,"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":["2027927|NM_174936.4(PCSK9):c.381T>G (p.Ser127Arg)|single nucleotide variant|Pathogenic|PCSK9|criteria provided, single submitter|1","2874|NM_174936.4(PCSK9):c.646T>C (p.Phe216Leu)|single nucleotide variant|Pathogenic|PCSK9|no assertion criteria provided|1","431555|NM_174936.4(PCSK9):c.42_43insTG (p.Leu15fs)|Insertion|Pathogenic|PCSK9|criteria provided, single submitter|1","440706|NM_174936.4(PCSK9):c.140C>G (p.Ser47Cys)|single nucleotide variant|Pathogenic|PCSK9|no assertion criteria provided|1","440712|NM_174936.4(PCSK9):c.248A>C (p.Lys83Thr)|single nucleotide variant|Pathogenic|PCSK9|no assertion criteria provided|1","440715|NM_174936.4(PCSK9):c.323T>C (p.Leu108Pro)|single nucleotide variant|Pathogenic|PCSK9|no assertion criteria provided|1","440721|NM_174936.4(PCSK9):c.1402A>G (p.Thr468Ala)|single nucleotide variant|Pathogenic|PCSK9|no assertion criteria provided|1","440722|NM_174936.4(PCSK9):c.1411G>T (p.Ala471Ser)|single nucleotide variant|Pathogenic|PCSK9|no assertion criteria provided|1","440725|NM_174936.4(PCSK9):c.2005G>C (p.Glu669Gln)|single nucleotide variant|Pathogenic|PCSK9|no assertion criteria provided|1"]}]}