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