ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5265C>T (p.Ser1755=)

dbSNP: rs1555576855
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000508645 SCV000605911 uncertain significance not specified 2017-01-16 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001183220 SCV001348895 likely benign Hereditary cancer-predisposing syndrome 2018-11-20 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV001077101 SCV001242973 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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