ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.1683T>C (p.Ser561=)

dbSNP: rs1567798735
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000758789 SCV000887631 uncertain significance not provided 2018-10-24 criteria provided, single submitter clinical testing
Invitae RCV003645085 SCV004396409 likely benign Hereditary breast ovarian cancer syndrome 2023-09-26 criteria provided, single submitter clinical testing

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