ClinVar Miner

Submissions for variant NM_001851.6(COL9A1):c.14+133G>A

gnomAD frequency: 0.01008  dbSNP: rs113812077
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001592408 SCV001824014 likely benign not provided 2018-07-15 criteria provided, single submitter clinical testing

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