Submissions for variant NM_000179.3(MSH6):c.4002-10dup

dbSNP: rs59056100

Total submissions: 9

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Mendelics	RCV000986749	SCV001135864	benign	Lynch syndrome 5	2019-05-28	criteria provided, single submitter	clinical testing
GeneDx	RCV001529654	SCV001941899	benign	not provided	2019-11-19	criteria provided, single submitter	clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital	RCV001692331	SCV002568083	likely benign	not specified	2023-08-15	criteria provided, single submitter	clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario	RCV003150375	SCV003837662	benign	Breast and/or ovarian cancer	2021-07-21	criteria provided, single submitter	clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano	RCV001529654	SCV004222029	benign	not provided	2023-02-27	criteria provided, single submitter	clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV001529654	SCV001743472	likely benign	not provided		no assertion criteria provided	clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute	RCV001692331	SCV001906370	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center	RCV001692331	SCV001964032	benign	not specified		no assertion criteria provided	clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht	RCV001692331	SCV001978312	benign	not specified		no assertion criteria provided	clinical testing