ClinVar Miner

Submissions for variant NM_033100.4(CDHR1):c.56-86C>T

gnomAD frequency: 0.00979  dbSNP: rs148784005
Minimum review status: Collection method:
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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 RCV001557243 SCV001778970 likely benign not provided 2019-10-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001557243 SCV005221784 likely benign not provided criteria provided, single submitter not provided

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