ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.1428T>C (p.His476=)

dbSNP: rs1060504572
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001500498 SCV001705288 likely benign Hereditary breast ovarian cancer syndrome 2016-07-12 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001805091 SCV002052585 likely benign Hereditary cancer-predisposing syndrome 2021-05-18 criteria provided, single submitter clinical testing

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