ClinVar Miner

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

dbSNP: rs373413425
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Total submissions: 6
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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
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

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