ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.3930A>C (p.Thr1310=)

dbSNP: rs1555586780
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000584642 SCV000688457 likely benign Hereditary cancer-predisposing syndrome 2017-09-14 criteria provided, single submitter clinical testing
Invitae RCV000933840 SCV001079549 likely benign Hereditary breast ovarian cancer syndrome 2023-09-24 criteria provided, single submitter clinical testing

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