ClinVar Miner

Submissions for variant NM_001854.4(COL11A1):c.652-6_652-5insTTC

dbSNP: rs749687230
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001516509 SCV001724802 benign not provided 2024-01-24 criteria provided, single submitter clinical testing
GeneDx RCV001516509 SCV001769832 likely benign not provided 2019-09-15 criteria provided, single submitter clinical testing

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