ClinVar Miner

Submissions for variant NM_024529.5(CDC73):c.1418-7T>C

dbSNP: rs2102073224
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002185556 SCV002354564 likely benign Parathyroid carcinoma 2025-01-24 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004543725 SCV004765036 likely benign CDC73-related disorder 2022-04-11 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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