ClinVar Miner

Submissions for variant NM_033100.4(CDHR1):c.55+46A>G

gnomAD frequency: 0.01610  dbSNP: rs115146172
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 RCV001609661 SCV001837674 benign not provided 2019-10-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001609661 SCV005317550 benign not provided criteria provided, single submitter not provided

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