ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.2203C>T (p.Leu735=)

dbSNP: rs587781781
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000526532 SCV000635835 likely benign Hereditary breast ovarian cancer syndrome 2023-04-23 criteria provided, single submitter clinical testing

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