ClinVar Miner

Submissions for variant NM_001854.4(COL11A1):c.3258T>C (p.Ala1086=)

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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 RCV003041010 SCV003353750 likely benign not provided 2023-12-11 criteria provided, single submitter clinical testing

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