ClinVar Miner

Submissions for variant NM_000138.5(FBN1):c.1941G>C (p.Leu647=)

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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 RCV004014713 SCV004827663 likely benign Marfan syndrome 2023-05-16 criteria provided, single submitter clinical testing

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