ClinVar Miner

Submissions for variant NM_001844.5(COL2A1):c.970-205T>C

gnomAD frequency: 0.20253  dbSNP: rs2071437
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
GeneDx RCV001667690 SCV001886939 benign not provided 2018-06-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001667690 SCV005232902 benign not provided criteria provided, single submitter not provided

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