ClinVar Miner

Submissions for variant NM_000138.5(FBN1):c.1668G>C (p.Val556=)

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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 RCV004803836 SCV005424903 likely benign Marfan syndrome 2024-04-16 criteria provided, single submitter clinical testing

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