Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 May 18:2024:3043736.
doi: 10.1155/2024/3043736. eCollection 2024.

Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes- ENG and ACVRL1

Affiliations

Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes- ENG and ACVRL1

Desiree DeMille et al. Hum Mutat. .

Abstract

The 2015 ACMG/AMP standards and guidelines for interpretation of sequence variants are widely used by laboratories, including for variant curation of the hereditary hemorrhagic telangiectasia (HHT) genes. However, the need for gene- and disease-specific modifications and specifications of these general guidelines to optimize and standardize variant classification was recognized at the time of publication. With this goal, the ClinGen HHT variant curation expert panel was formed. Here, we describe our recommended HHT-specific variant classification criteria and the outcomes from pilot testing of 30 variants of the ENG and ACVRL1 genes. Eight of the original ACMG/AMP rules were determined to not be applicable for ENG- or ACVRL1-related HHT or were previously recommended by ClinGen for removal, two rules were unmodified, and the remaining 18 rules were modified according to HHT specifications or previous ClinGen general recommendations. This study demonstrates the importance of HHT-specific criteria in the optimization and standardization of HHT variant classification and conflicting classification resolution.

PubMed Disclaimer

Conflict of interest statement

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Figures

Figure 1
Figure 1
HHT PVS1 decision tree adapted from Abou Tayoun et al. [35].

References

    1. Richards S., Aziz N., Bale S., et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genetics in Medicine . 2015;17(5):405–424. doi: 10.1038/gim.2015.30. - DOI - PMC - PubMed
    1. Faughnan M. E., Mager J. J., Hetts S. W., et al. Second international guidelines for the diagnosis and management of hereditary hemorrhagic telangiectasia. Annals of Internal Medicine . 2020;173(12):989–1001. doi: 10.7326/M20-1443. - DOI - PubMed
    1. Porteous M. E., Burn J., Proctor S. J. Hereditary haemorrhagic telangiectasia: a clinical analysis. Journal of Medical Genetics . 1992;29(8):527–530. doi: 10.1136/jmg.29.8.527. - DOI - PMC - PubMed
    1. Anderson E., Sharma L., Alsafi A., Shovlin C. L. Pulmonary arteriovenous malformations may be the only clinical criterion present in genetically confirmed hereditary haemorrhagic telangiectasia. Thorax . 2022;77(6):628–630. doi: 10.1136/thoraxjnl-2021-218332. - DOI - PMC - PubMed
    1. Bayrak-Toydemir P., McDonald J., Markewitz B., et al. Genotype-phenotype correlation in hereditary hemorrhagic telangiectasia: mutations and manifestations. American Journal of Medical Genetics. Part A . 2006;140(5):463–470. doi: 10.1002/ajmg.a.31101. - DOI - PubMed

MeSH terms

LinkOut - more resources