ClinVar Miner

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

gnomAD frequency: 0.00010  dbSNP: rs150571620
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
Eurofins Ntd Llc (ga) RCV000728039 SCV000855562 uncertain significance not provided 2017-07-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000728039 SCV001679876 likely benign not provided 2024-10-02 criteria provided, single submitter clinical testing

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