Submissions for variant NM_024675.4(PALB2):c.1684+18TGA[9]

dbSNP: rs368593832

Total submissions: 7

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
GeneDx	RCV001529629	SCV001814183	likely benign	not provided	2019-08-11	criteria provided, single submitter	clinical testing
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State	RCV002225297	SCV002504932	likely benign	Hereditary breast ovarian cancer syndrome	2022-04-19	criteria provided, single submitter	clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital	RCV002267851	SCV002551674	likely benign	not specified	2023-08-15	criteria provided, single submitter	clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario	RCV003149777	SCV003838716	benign	Breast and/or ovarian cancer	2021-06-29	criteria provided, single submitter	clinical testing
Leiden Open Variation Database	RCV001030248	SCV001193140	likely benign	Familial cancer of breast	2020-02-28	no assertion criteria provided	curation	Curators: Marc Tischkowitz, Arleen D. Auerbach. Submitter to LOVD: Marc Tischkowitz.
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	RCV001529629	SCV001743410	likely benign	not provided		no assertion criteria provided	clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute	RCV001529629	SCV001906204	likely benign	not provided		no assertion criteria provided	clinical testing