ClinVar Miner

Submissions for variant NM_024529.5(CDC73):c.370+17A>G

gnomAD frequency: 0.00001  dbSNP: rs760583012
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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 RCV002144828 SCV002416898 likely benign Parathyroid carcinoma 2023-10-14 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500088 SCV002807045 likely benign Hyperparathyroidism 1; Parathyroid carcinoma; Hyperparathyroidism 2 with jaw tumors 2022-05-27 criteria provided, single submitter clinical testing

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