ClinVar Miner

Submissions for variant NM_007299.4(BRCA1):c.-19-10T>C (rs201866997)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000503454 SCV000591227 benign not specified 2015-01-08 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000503454 SCV000602712 benign not specified 2016-12-01 criteria provided, single submitter clinical testing
Color RCV000581644 SCV000688309 likely benign Hereditary cancer-predisposing syndrome 2015-08-26 criteria provided, single submitter clinical testing
Breast Cancer Information Core (BIC) (BRCA1) RCV000111494 SCV000143936 not provided Breast-ovarian cancer, familial 1 no assertion provided clinical testing

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