ClinVar Miner

Submissions for variant NM_000138.5(FBN1):c.7825A>G (p.Asn2609Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004009769 SCV004824112 uncertain significance Marfan syndrome 2023-03-04 criteria provided, single submitter clinical testing

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