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

Desiree Demille, Jamie McDonald, Carmelo Bernabeu, Hilary Racher, Carla Olivieri, Claudia Cantarini, Anna Sbalchiero, Bryony A. Thompson, Luca Jovine, Claire L. Shovlin, Sophie Dupuis-Girod, Gaetan Lesca, Maud Tusseau, Arupa Ganguly, Raj S. Kasthuri, Jaime Jessen, Maarten P.G. Massink, Shoji Ichikawa, Pinar Bayrak-Toydemir*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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.

Original languageEnglish
Article number3043736
JournalHuman mutation
Volume2024
DOIs
Publication statusPublished - 2024

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