ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.7482+64C>T

dbSNP: rs74145677
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 RCV001541533 SCV001759546 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001541533 SCV005321824 benign not provided criteria provided, single submitter not provided

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