ClinVar Miner

Submissions for variant NM_024529.5(CDC73):c.1031-18T>G

gnomAD frequency: 0.00001  dbSNP: rs1322891058
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002195780 SCV002486780 likely benign Parathyroid carcinoma 2024-05-22 criteria provided, single submitter clinical testing

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