ClinVar Miner

Submissions for variant NM_000059.3(BRCA2):c.8488-1_8489delinsTCCATTACA (rs886038183)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomics Laboratory,Virgen de la Arrixaca University Clinical Hospital RCV000785643 SCV000886517 likely pathogenic Hereditary breast and ovarian cancer syndrome 2019-02-21 criteria provided, single submitter clinical testing

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