| Literature DB >> 31479589 |
Steven M Harrison1,2, Leslie G Biesecker3, Heidi L Rehm1,2,4.
Abstract
The 2015 ACMG/AMP guidelines established a classification system for sequence variants; however, the broad scope of these guidelines necessitates specification of evidence types for specific genes or diseases of interest. Since publication of the guidelines, both general use and disease-focused specifications have emerged to aid in accurate application of ACMG/AMP evidence types. This article summarizes the approaches to, and rationale for, specifying three evidence categories (population frequency data, variant type and location, and case-level data), including available resources and a quantitative framework that can inform the specification process.Entities:
Keywords: ACMG/AMP guidelines; clinical genetics; variant interpretation
Mesh:
Year: 2019 PMID: 31479589 PMCID: PMC6885382 DOI: 10.1002/cphg.93
Source DB: PubMed Journal: Curr Protoc Hum Genet ISSN: 1934-8258