ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.1134+113C>T

gnomAD frequency: 0.05138  dbSNP: rs75714857
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 RCV001616549 SCV001840301 benign not provided 2018-07-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001616549 SCV005321722 benign not provided criteria provided, single submitter not provided

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