Submissions for variant NM_007294.4(BRCA1):c.441+36_441+49del

dbSNP: rs373413425

Total submissions: 8

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Michigan Medical Genetics Laboratories, University of Michigan	RCV000211009	SCV000195882	benign	Breast-ovarian cancer, familial, susceptibility to, 1	2014-11-03	criteria provided, single submitter	clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	RCV000506984	SCV000602703	benign	not specified	2016-11-04	criteria provided, single submitter	clinical testing
Mendelics	RCV000211009	SCV001140635	benign	Breast-ovarian cancer, familial, susceptibility to, 1	2019-05-28	criteria provided, single submitter	clinical testing
GeneDx	RCV001711989	SCV001939539	benign	not provided	2019-08-19	criteria provided, single submitter	clinical testing
Fulgent Genetics, Fulgent Genetics	RCV002485374	SCV002798626	benign	Familial cancer of breast; Breast-ovarian cancer, familial, susceptibility to, 1; Pancreatic cancer, susceptibility to, 4; Fanconi anemia, complementation group S	2021-11-12	criteria provided, single submitter	clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital	RCV000506984	SCV005089853	likely benign	not specified	2025-03-04	criteria provided, single submitter	clinical testing
Clinical Genetics Laboratory, Department of Pathology, Netherlands Cancer Institute	RCV000506984	SCV001977616	benign	not specified		no assertion criteria provided	clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht	RCV001711989	SCV001977874	likely benign	not provided		no assertion criteria provided	clinical testing