ClinVar Miner

Submissions for variant NM_024529.5(CDC73):c.308-16C>A

gnomAD frequency: 0.00252  dbSNP: rs201766013
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244700 SCV000314344 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058332 SCV002405643 benign Parathyroid carcinoma 2024-02-01 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500920 SCV002811190 benign Hyperparathyroidism 1; Parathyroid carcinoma; Hyperparathyroidism 2 with jaw tumors 2021-07-21 criteria provided, single submitter clinical testing

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