ClinVar Miner

Submissions for variant NM_024529.5(CDC73):c.1559+20A>G

gnomAD frequency: 0.00001  dbSNP: rs1281829953
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002100932 SCV002389291 likely benign Parathyroid carcinoma 2024-01-10 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486868 SCV002799463 likely benign Hyperparathyroidism 1; Parathyroid carcinoma; Hyperparathyroidism 2 with jaw tumors 2022-05-19 criteria provided, single submitter clinical testing

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