ClinVar Miner

Submissions for variant NM_001854.4(COL11A1):c.2105C>A (p.Pro702His)

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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 RCV005177698 SCV005805522 likely benign not provided 2024-08-29 criteria provided, single submitter clinical testing

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