{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":11,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:613","source":"HGNC:613|apolipoprotein E","targets":["126456|NM_000041.4(APOE):c.497TCC[1] (p.Leu167del)|Microsatellite|Pathogenic|APOE|criteria provided, multiple submitters, no conflicts|19","17849|NM_000041.4(APOE):c.61G>A (p.Glu21Lys)|single nucleotide variant|Pathogenic|APOE|no assertion criteria provided|19","17852|NM_000041.4(APOE):c.237-2A>G|single nucleotide variant|Pathogenic|APOE|no assertion criteria provided|19","17853|NM_000041.4(APOE):c.415_435dup (p.Glu139_Gly145dup)|Duplication|Pathogenic|APOE|no assertion criteria provided|19","17857|NM_000041.4(APOE):c.490A>G (p.Lys164Glu)|single nucleotide variant|Pathogenic|APOE|no assertion criteria provided|19","17858|NM_000041.4(APOE):c.490A>C (p.Lys164Gln)|single nucleotide variant|Pathogenic|APOE|no assertion criteria provided|19","17859|NM_000041.4(APOE):c.736C>T (p.Arg246Cys)|single nucleotide variant|Pathogenic|APOE|no assertion criteria provided|19","17861|NM_000041.4(APOE):c.146del (p.Gly49fs)|Deletion|Pathogenic|APOE|no assertion criteria provided|19","17874|NM_000041.4(APOE):c.455G>A (p.Arg152Gln)|single nucleotide variant|Pathogenic|APOE|no assertion criteria provided|19","17875|NM_000041.4(APOE):c.875G>A (p.Arg292His)|single nucleotide variant|Pathogenic|APOE|no assertion criteria provided|19","17879|NM_000041.4(APOE):c.488G>C (p.Arg163Pro)|single nucleotide variant|Pathogenic|APOE|no assertion criteria provided|19"]}]}