Submissions for variant NM_000251.3(MSH2):c.212-4del

dbSNP: rs746333570

Total submissions: 8

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Ambry Genetics	RCV000162526	SCV000212923	likely benign	Hereditary cancer-predisposing syndrome	2018-03-01	criteria provided, single submitter	clinical testing	Other strong data supporting benign classification
Color Diagnostics, LLC DBA Color Health	RCV000162526	SCV000685013	likely benign	Hereditary cancer-predisposing syndrome	2015-02-13	criteria provided, single submitter	clinical testing
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden	RCV001355133	SCV002009336	benign	not provided	2021-11-03	criteria provided, single submitter	clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital	RCV001706068	SCV002552189	likely benign	not specified	2023-08-15	criteria provided, single submitter	clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center	RCV000625491	SCV000745630	benign	Lynch syndrome 1	2015-05-13	no assertion criteria provided	clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System	RCV001355133	SCV001549922	uncertain significance	not provided		no assertion criteria provided	clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute	RCV001706068	SCV001906381	benign	not specified		no assertion criteria provided	clinical testing
Clinical Genetics, Academic Medical Center	RCV001706068	SCV001917774	benign	not specified		no assertion criteria provided	clinical testing