ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.208G>C (p.Gly70Arg)

dbSNP: rs764349043
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000666377 SCV000790658 uncertain significance Hyperinsulinemic hypoglycemia, familial, 1 2017-03-31 criteria provided, single submitter clinical testing
Molecular Genetics, Madras Diabetes Research Foundation RCV002051877 SCV002318414 uncertain significance Neonatal diabetes mellitus criteria provided, single submitter clinical testing
Baylor Genetics RCV003465451 SCV004207427 likely pathogenic Type 2 diabetes mellitus 2023-02-14 criteria provided, single submitter clinical testing

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