{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":6,"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":["1936|NM_198578.4(LRRK2):c.4321C>G (p.Arg1441Gly)|single nucleotide variant|Pathogenic|LRRK2|criteria provided, multiple submitters, no conflicts|12","1937|NM_198578.4(LRRK2):c.5096A>G (p.Tyr1699Cys)|single nucleotide variant|Pathogenic|LRRK2|no assertion criteria provided|12","1938|NM_198578.4(LRRK2):c.4321C>T (p.Arg1441Cys)|single nucleotide variant|Pathogenic|LRRK2|criteria provided, multiple submitters, no conflicts|12","1939|NM_198578.4(LRRK2):c.3364A>G (p.Ile1122Val)|single nucleotide variant|Pathogenic|LRRK2|no assertion criteria provided|12","1941|NM_198578.4(LRRK2):c.6059T>C (p.Ile2020Thr)|single nucleotide variant|Pathogenic|LRRK2|criteria provided, single submitter|12","2572065|NM_198578.4(LRRK2):c.4969C>T (p.Gln1657Ter)|single nucleotide variant|Pathogenic|LRRK2|no assertion criteria provided|12"]}]}