ClinVar Miner

Submissions for variant NM_004752.4(GCM2):c.1398G>C (p.Glu466Asp)

dbSNP: rs537546612
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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 RCV002272601 SCV002556444 uncertain significance Hyperparathyroidism 4 2021-07-16 criteria provided, single submitter clinical testing

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