ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.901C>A (p.Arg301=)

dbSNP: rs397517364
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
Invitae RCV003708591 SCV004477150 likely benign not provided 2022-12-09 criteria provided, single submitter clinical testing
Natera, Inc. RCV001280192 SCV001467352 uncertain significance Usher syndrome type 1 2020-04-11 no assertion criteria provided clinical testing

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