ClinVar Miner

Submissions for variant NM_024529.5(CDC73):c.132-17T>G

dbSNP: rs2103113863
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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 RCV002135291 SCV002449799 likely benign Parathyroid carcinoma 2023-03-21 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494418 SCV002803320 likely benign Hyperparathyroidism 1; Parathyroid carcinoma; Hyperparathyroidism 2 with jaw tumors 2021-10-20 criteria provided, single submitter clinical testing

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