ClinVar Miner

Submissions for variant NM_001854.4(COL11A1):c.652-18_652-16dup

dbSNP: rs36076089
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001530210 SCV001744930 benign not provided 2019-08-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001530210 SCV002404439 benign not provided 2025-01-29 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001530210 SCV001798460 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579880 SCV001808831 benign not specified no assertion criteria provided clinical testing

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