ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.1844C>G (p.Ser615Cys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV004764459 SCV005373888 uncertain significance Hyperinsulinemic hypoglycemia, familial, 1 2024-09-22 criteria provided, single submitter clinical testing

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