ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.2689G>T (p.Asp897Tyr)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004587701 SCV005076204 uncertain significance not specified 2024-04-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005051454 SCV005676328 likely pathogenic Diabetes mellitus, transient neonatal, 2; Hyperinsulinemic hypoglycemia, familial, 1; Leucine-induced hypoglycemia; Type 2 diabetes mellitus; Diabetes mellitus, permanent neonatal 3 2024-04-25 criteria provided, single submitter clinical testing

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