ClinVar Miner

Submissions for variant NM_000090.4(COL3A1):c.2022+14T>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003861148 SCV004669441 likely benign Ehlers-Danlos syndrome, type 4 2023-08-14 criteria provided, single submitter clinical testing

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