ClinVar Miner

Submissions for variant NM_001853.4(COL9A3):c.663C>T (p.Leu221=)

gnomAD frequency: 0.00003  dbSNP: rs996170616
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 RCV002082597 SCV002322671 likely benign not provided 2024-10-16 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004587297 SCV005076424 likely benign not specified 2024-04-26 criteria provided, single submitter clinical testing

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