ClinVar Miner

Submissions for variant NM_001844.5(COL2A1):c.1735-24T>C

gnomAD frequency: 0.05260  dbSNP: rs41317933
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000243008 SCV000308073 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001683028 SCV001897160 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001683028 SCV005230709 benign not provided criteria provided, single submitter not provided

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