ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.5234A>G (p.Asn1745Ser)

dbSNP: rs1567764456
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000679700 SCV000806968 uncertain significance not provided 2017-12-21 criteria provided, single submitter clinical testing
Brotman Baty Institute, University of Washington RCV001077064 SCV001242927 not provided Breast-ovarian cancer, familial, susceptibility to, 1 no assertion provided in vitro

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