ClinVar Miner

Submissions for variant NM_024529.5(CDC73):c.69C>G (p.Asp23Glu)

dbSNP: rs1675465120
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV002272699 SCV002556734 uncertain significance Hyperparathyroidism 1 2021-05-25 criteria provided, single submitter clinical testing

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