ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.9183C>T (p.Asp3061=)

dbSNP: rs1841920632
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001464276 SCV001668242 likely benign not provided 2022-10-10 criteria provided, single submitter clinical testing

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