The ACMG/AMP reputable source criteria for the interpretation of sequence variants
Genet Med
.
2018 Dec;20(12):1687-1688.
doi: 10.1038/gim.2018.42.
Authors
Leslie G Biesecker
1
,
Steven M Harrison
2
;
ClinGen Sequence Variant Interpretation Working Group
Affiliations
1
Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.
2
Partners HealthCare Laboratory for Molecular Medicine and Harvard Medical School, Boston, Massachusetts, USA. sharrison@bwh.harvard.edu.
PMID:
29543229
PMCID:
PMC6709533
DOI:
10.1038/gim.2018.42
No abstract available
Publication types
Letter
Comment
MeSH terms
Adenosine Monophosphate
Consensus
Genetics, Medical*
Genomics
Pathology, Molecular*
United States
Substances
Adenosine Monophosphate
Grant support
U41 HG006834/HG/NHGRI NIH HHS/United States