ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.68-44T>C

gnomAD frequency: 0.02198  dbSNP: rs79513610
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 RCV001713599 SCV001942197 benign not provided 2018-06-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001713599 SCV005319530 benign not provided criteria provided, single submitter not provided

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