ClinVar Miner

Submissions for variant NM_024529.5(CDC73):c.908-6dup

dbSNP: rs563805986
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002103031 SCV002388904 benign Parathyroid carcinoma 2024-01-03 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256915 SCV002530573 likely benign Hereditary cancer-predisposing syndrome 2021-07-02 criteria provided, single submitter curation

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