Folklore Clinical Variant Interpretation

Folklore is Helena Bioinformatics' clinical variant interpretation platform for supported GRCh38 germline SNVs and simple indels. It combines variant resolution, annotation, automated ACMG/AMP classification, evidence, phenotype context, prioritisation and source-linked scientific literature in one reviewable record. Folklore supports qualified genetics professionals and does not replace professional review, provide diagnosis or treatment advice, or accept patient and private case data through its public interfaces.