ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.8179-138C>T

gnomAD frequency: 0.01261  dbSNP: rs7085713
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001547511 SCV001767238 likely benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001547511 SCV005228232 likely benign not provided criteria provided, single submitter not provided

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