{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely pathogenic\"]","source_dataset":"hgnc","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":"HGNC:18618","source":"HGNC:18618|leucine rich repeat kinase 2","targets":["225276|NM_198578.4(LRRK2):c.4321C>A (p.Arg1441Ser)|single nucleotide variant|Likely pathogenic|LRRK2|criteria provided, single submitter|12","3341978|NM_198578.4(LRRK2):c.4318G>C (p.Ala1440Pro)|single nucleotide variant|Likely pathogenic|LRRK2|criteria provided, single submitter|12"]}]}