{"query":"chr11 5227002 T A","kind":"canonical","recognisedAs":"Variant ID","results":[{"kind":"variant","id":"11-5227002-T-A","route":"/variant/11-5227002-T-A/","label":"11-5227002-T-A","description":"SNV · from Genomic position and alleles"}],"semantic":{"query":"chr11 5227002 T A","isNaturalLanguage":true,"matchedPhenotypes":[],"candidateGenes":[],"clinicalReasoning":"No direct clinical phenotype features detected for \"chr11 5227002 T A\". Try clinical terms such as \"recurrent seizures\", \"ataxia\", \"microcephaly\", or \"hepatosplenomegaly\".","suggestedTargets":[]}}