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How does re-classification of variants of unknown significance (VUS) impact the management of patien...

How does re-classification of variants of unknown significance (VUS) impact the management of patien...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7783bc06d4f8473ebd28c6a2080cce23

How does re-classification of variants of unknown significance (VUS) impact the management of patients at risk for hereditary breast cancer?

About this item

Full title

How does re-classification of variants of unknown significance (VUS) impact the management of patients at risk for hereditary breast cancer?

Publisher

England: BioMed Central Ltd

Journal title

BMC medical genomics, 2022-05, Vol.15 (1), p.122-122, Article 122

Language

English

Formats

Publication information

Publisher

England: BioMed Central Ltd

More information

Scope and Contents

Contents

The popularity of multigene testing increases the probability of identifying variants of uncertain significance (VUS). While accurate variant interpretation enables clinicians to be better informed of the genetic risk of their patients, currently, there is a lack of consensus management guidelines for clinicians on VUS.
Among the BRCA1 and BRCA2...

Alternative Titles

Full title

How does re-classification of variants of unknown significance (VUS) impact the management of patients at risk for hereditary breast cancer?

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_7783bc06d4f8473ebd28c6a2080cce23

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_7783bc06d4f8473ebd28c6a2080cce23

Other Identifiers

ISSN

1755-8794

E-ISSN

1755-8794

DOI

10.1186/s12920-022-01270-4

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