ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.2712G>A (p.Pro904=)

gnomAD frequency: 0.00001  dbSNP: rs570110527
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 RCV000940967 SCV001086839 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Natera, Inc. RCV001275945 SCV001461625 benign Usher syndrome type 1 2020-04-15 no assertion criteria provided clinical testing

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