ClinVar Miner

Submissions for variant NM_000090.4(COL3A1):c.1794C>T (p.Gly598=)

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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 RCV004015705 SCV004836286 likely benign Ehlers-Danlos syndrome, type 4 2023-12-18 criteria provided, single submitter clinical testing

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