ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.61del (p.Val21fs)

dbSNP: rs2133737961
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics, Madras Diabetes Research Foundation RCV002052035 SCV002318427 likely pathogenic Hyperinsulinemic hypoglycemia, familial, 1 criteria provided, single submitter clinical testing
Baylor Genetics RCV004572012 SCV005058574 pathogenic Type 2 diabetes mellitus 2024-03-28 criteria provided, single submitter clinical testing

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