ClinVar Miner

Submissions for variant NM_022124.6(CDH23):c.882C>G (p.Thr294=)

gnomAD frequency: 0.00001  dbSNP: rs752615081
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 RCV002075580 SCV002387971 likely benign not provided 2024-10-29 criteria provided, single submitter clinical testing

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