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Need for revision of the ACMG/AMP guidelines for interpretation of X-linked variants.
Inoue, Yoko; Machida, Osamu; Kita, Yosuke; Yamamoto, Toshiyuki.
Afiliação
  • Inoue Y; Division of Gene Medicine, Graduate School of Medical Science, Tokyo Women's Medical University, Tokyo, Japan.
  • Machida O; Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan.
  • Kita Y; Division of Gene Medicine, Graduate School of Medical Science, Tokyo Women's Medical University, Tokyo, Japan.
  • Yamamoto T; Department of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
Intractable Rare Dis Res ; 11(3): 120-124, 2022 Aug.
Article em En | MEDLINE | ID: mdl-36200025
ABSTRACT
The guidelines provided by American College of Medical Genetics and Genomics (ACMG) and the Association of Molecular Pathology (AMP) (ACMG/AMP guidelines) suggest a framework for the classification of clinical variants. However, the interpretations can be inconsistent, with each definition sometimes proving to be ambiguous. In particular, there can be difficulty with interpretation of variants related to the X-linked recessive trait. To confirm whether there are biases in the interpretation of inherited traits, we reanalyzed variants reported prior to the release of the ACMG/AMP guidelines. As expected, the interpretation ratio as pathogenic or likely pathogenic was significantly lower for variants related to the X-linked recessive trait. Evaluation of variants related to the X-linked recessive trait, hence, need to consider whether the variant is identified only in males in accordance with the X-linked recessive trait. The ACMG/AMP guidelines should be revised to eliminate the bias revealed in this study.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Intractable Rare Dis Res Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline Idioma: En Revista: Intractable Rare Dis Res Ano de publicação: 2022 Tipo de documento: Article