{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":25,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:6018","source":"HGNC:6018|interleukin 6","targets":["1050490|NC_000007.14:g.22725249C>A|single nucleotide variant|Uncertain significance|IL6|no assertion criteria provided|7","14718|NC_000007.14:g.22727026C>G|single nucleotide variant|other; risk factor|IL6|no assertion criteria provided|7","14719|NC_000007.14:g.22726602A>G|single nucleotide variant|Benign|IL6|no assertion criteria provided|7","2245276|NM_000600.5(IL6):c.119C>A (p.Ala40Asp)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","2303034|NM_000600.5(IL6):c.620G>C (p.Arg207Thr)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","2406494|NM_000600.5(IL6):c.285G>C (p.Met95Ile)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","2495660|NM_000600.5(IL6):c.168A>C (p.Gln56His)|single nucleotide variant|Likely benign|IL6|criteria provided, single submitter|7","2534860|NM_000600.5(IL6):c.549C>A (p.Asn183Lys)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","2684485|GRCh37/hg19 7p15.3(chr7:22532986-22837871)x3|copy number gain|Uncertain significance|IL6|criteria provided, single submitter|7","3056054|NM_000600.5(IL6):c.603C>T (p.Phe201=)|single nucleotide variant|Benign|IL6|no assertion criteria provided|7","3285905|NM_000600.5(IL6):c.326A>G (p.Glu109Gly)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","3860355|NM_000600.5(IL6):c.533A>C (p.Lys178Thr)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","3860356|NM_000600.5(IL6):c.218A>G (p.Asn73Ser)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","3860357|NM_000600.5(IL6):c.586C>A (p.Arg196Ser)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","4038473|NM_000600.5(IL6):c.422G>T (p.Arg141Ile)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","4038474|NM_000600.5(IL6):c.163A>G (p.Lys55Glu)|single nucleotide variant|Likely benign|IL6|criteria provided, single submitter|7","4275185|NM_000600.5(IL6):c.261A>C (p.Glu87Asp)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","4290280|NM_000600.5(IL6):c.325del|Deletion||IL6||7","4336201|NM_000600.5(IL6):c.324+2T>C|single nucleotide variant||IL6||7","4678713|NM_000600.5(IL6):c.175T>C (p.Tyr59His)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","4678714|NM_000600.5(IL6):c.470A>C (p.Lys157Thr)|single nucleotide variant|Uncertain significance|IL6|criteria provided, single submitter|7","709119|NM_000600.5(IL6):c.91C>A (p.Pro31Thr)|single nucleotide variant|Benign|IL6|criteria provided, single submitter|7","717506|NM_000600.5(IL6):c.183C>T (p.Leu61=)|single nucleotide variant|Likely benign|IL6|criteria provided, multiple submitters, no conflicts|7","768143|NM_000600.5(IL6):c.94C>T (p.Pro32Ser)|single nucleotide variant|Benign|IL6|criteria provided, single submitter|7","777811|NM_000600.5(IL6):c.485A>T (p.Asp162Val)|single nucleotide variant|Benign|IL6|criteria provided, multiple submitters, no conflicts|7"]}]}