ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.4105G>A (p.Ala1369Thr)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003851783 SCV004660303 likely benign not provided 2022-12-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005051407 SCV005683381 uncertain significance Diabetes mellitus, transient neonatal, 2; Hyperinsulinemic hypoglycemia, familial, 1; Leucine-induced hypoglycemia; Type 2 diabetes mellitus; Diabetes mellitus, permanent neonatal 3 2024-04-10 criteria provided, single submitter clinical testing

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