ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.2976G>T (p.Thr992=)

dbSNP: rs553405751
Minimum review status: Collection method:
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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 RCV001398517 SCV001600290 likely benign not provided 2024-02-24 criteria provided, single submitter clinical testing

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