medRxivGenetic & Genomic MedicinePreprint
Consultation informs strategies to improve functional evidence use in variant classification
Rehan Marie VillaniiD, Bronwyn TerrilliD, Emma TudiniiD, Maddison E. McKenzieiD, Corrina C. CliffeiD, Christopher Norman HahniD, Ben LundieiD, Tessa MattiskeiD, Ebony MatotekiD, Abbye E. McEweniD, Sarah L. NickersoniD, James BreeniD, Douglas M. FowleriD, John ChristodoulouiD, Lea M. StaritaiD, Alan F. RubiniD, Amanda B. SpurdleiD
Abstract
To determine if a variant identified by diagnostic genetic testing is causal for disease, applied genetics professionals evaluate all available evidence to assign a clinical classification. Experimental assay data can provide strong functional evidence for or against pathogenicity in variant classification, but appears to be underutilised. We surveyed genetic diagnostic professionals in Australasia to assess their application of functional evidence in clinical practice. Results indicated that survey respondents are not confident to apply functional evidence, mainly due to uncertainty around practice recommendations. Respondents also identified need for support resources, educational opportunities, and in particular requested expert recommendations and updated practice guidelines to improve translation of experimental data to curation evidence. As an initial step, we have collated a list of functional assays recommended by 19 ClinGen Variant Curation Expert Panels as a source of international expert opinion on functional evidence evaluation. Additional support resources for diagnostic practice are in development.
- Citations
- 3
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A Comparative Survey of Functional Evidence Use in Hearing and Vision Loss Genetics
R. Arda Inan, Marina T. DiStefano, … Barbara Vona·Communications MedicinePeer-reviewed·May 30, 2026
- Workshops to improve use of functional evidence build confidence and suggest a practice development approach.
Rehan Marie Villani, Bronwyn Terrill, … Amanda B. Spurdle·medRxiv·Nov 10, 2025
- Insights on improving accessibility and usability of functional data to unlock its potential for variant interpretation
Min Seon Park, Runjun D. Kumar, … Andrew B. Stergachis·medRxiv·Jan 25, 2025
- Comparative analysis of functional assay evidence use by ClinGen Variant Curation Expert Panels
Dona Kanavy, Shannon M. McNulty, … Jonathan S. Berg·Genome MedicinePeer-reviewed·Nov 29, 2019
- Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework
Sarah E. Brnich, Ahmad N. Abou Tayoun, … Jonathan S. Berg·Genome MedicinePeer-reviewed·Dec 31, 2019
- Measuring the Meaning of Genomic Results: Harmonization of the Metric for Case-Level Results in the CSER2 Consortium
Bradford C. Powell, Laura M. Amendola, … Kevin M. Bowling·medRxiv·Jun 1, 2026