ClinVar Miner

Submissions for variant NM_001851.6(COL9A1):c.462A>T (p.Val154=)

dbSNP: rs150571620
Minimum review status: Collection method:
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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 RCV001465170 SCV001669153 likely benign not provided 2024-12-04 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004587161 SCV005075964 likely benign not specified 2024-04-01 criteria provided, single submitter clinical testing

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