Cargando…
ClinGen’s RASopathy Expert Panel Consensus Methods for Variant Interpretation
PURPOSE: Standardized and accurate variant assessment is essential for effective medical care. To that end, Clinical Genome (ClinGen) Resource clinical domain working groups (CDWG) are systematically reviewing disease-associated genes for sufficient evidence to support disease causality and creating...
Autores principales: | Gelb, Bruce D., Cavé, Hélène, Dillon, Mitchell W., Gripp, Karen W., Lee, Jennifer A., Mason-Suares, Heather, Rauen, Katherine A., Williams, Bradley, Zenker, Martin, Vincent, Lisa M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119537/ https://www.ncbi.nlm.nih.gov/pubmed/29493581 http://dx.doi.org/10.1038/gim.2018.3 |
Ejemplares similares
-
Comparative analysis of functional assay evidence use by ClinGen Variant Curation Expert Panels
por: Kanavy, Dona M., et al.
Publicado: (2019) -
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel
por: Shen, Jun, et al.
Publicado: (2019) -
Adaptation of ACMG-ClinGen Technical Standards for Copy Number Variant Interpretation Concordance
por: Zhang, Kuo, et al.
Publicado: (2022) -
Adapting the ACMG/AMP variant classification framework: A perspective from the ClinGen Hemoglobinopathy Variant Curation Expert Panel
por: Kountouris, Petros, et al.
Publicado: (2021) -
ClinGen Expert Clinical Validity Curation of 164 Hearing Loss Gene-Disease Pairs
por: DiStefano, Marina T., et al.
Publicado: (2019)