ClinVar Miner

Submissions for variant NM_007294.4(BRCA1):c.3111_3118del (p.Glu1038fs)

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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 RCV005360282 SCV005915369 pathogenic Fanconi anemia, complementation group S 2019-11-05 criteria provided, single submitter clinical testing

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