ClinVar Miner

Submissions for variant NM_000059.4(BRCA2):c.3849A>G (p.Val1283=)

dbSNP: rs1214830867
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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 RCV001181156 SCV001346250 likely benign Hereditary cancer-predisposing syndrome 2018-10-09 criteria provided, single submitter clinical testing
Invitae RCV001414130 SCV001616257 likely benign Hereditary breast ovarian cancer syndrome 2023-05-19 criteria provided, single submitter clinical testing

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