ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.3799del (p.Leu1267fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003461530 SCV004197208 likely pathogenic Fanconi anemia complementation group I 2023-03-17 criteria provided, single submitter clinical testing

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