Variant of uncertain significance - Alchetron, the free social encyclopedia
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Variant of uncertain significance - Alchetron, the free social encyclopedia
A variant of uncertain (or unknown) significance (VUS) is an allele, or variant form of a gene, which has been identified through genetic testing, but whose significance to the function or health of an organism is not known. Two related terms are Gene of uncertain significance (GUS), which refers
Aug 18, 2017
Genetic Testing and VUS
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🧬Learn all about genetic testing with Dr. Clair Francomano The Ehlers-Danlos syndromes (EDS) are a group of genetic connective tissue disorders. Each type of EDS is caused by pathogenic variants of genes that provide the instructions for making connective tissue proteins. Hypermobile EDS (hEDS) is the most common type of EDS, but the genetic cause(s) of hEDS are unknown. The other types of EDS are associated with specific pathogenic variants. Genetic testing is available for every type of EDS e
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🧬Learn all about genetic testing with Dr. Clair Francomano The Ehlers-Danlos syndromes (EDS) are a group of genetic connective tissue disorders. Each type of EDS is caused by pathogenic variants of genes that provide the instructions for making connective tissue proteins. Hypermobile EDS (hEDS) is the most common type of EDS, but the genetic cause(s) of hEDS are unknown. The other types of EDS are associated with specific pathogenic variants. Genetic testing is available for every type of EDS e
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