ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5052T>G (p.Thr1684=)

dbSNP: rs760922019
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001473744 SCV001677901 likely benign Hereditary breast ovarian cancer syndrome 2020-07-26 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV001077973 SCV001243988 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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