{"query":"1 55516888 rs11591147 G T . PASS .","kind":"vcf-line","recognisedAs":"VCF line","results":[{"kind":"variant","id":"1-55516888-G-T","route":"/variant/1-55516888-G-T/","label":"1-55516888-G-T","description":"VCF 1 55516888 G T · rs11591147"}],"semantic":{"query":"1 55516888 rs11591147 G T . PASS .","isNaturalLanguage":true,"matchedPhenotypes":[],"candidateGenes":[],"clinicalReasoning":"No direct clinical phenotype features detected for \"1 55516888 rs11591147 G T . PASS .\". Try clinical terms such as \"recurrent seizures\", \"ataxia\", \"microcephaly\", or \"hepatosplenomegaly\".","suggestedTargets":[]}}