ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.1410_1416delinsTTGGGG (p.Leu471fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005365540 SCV005914249 pathogenic Fanconi anemia, complementation group S 2020-09-24 criteria provided, single submitter clinical testing

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