ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.4308T>A (p.Ser1436=)

dbSNP: rs1060915
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001516393 SCV001724666 benign Hereditary breast ovarian cancer syndrome 2020-06-28 criteria provided, single submitter clinical testing

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