ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.643G>A (p.Val215Ile)

dbSNP: rs2133680286
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics, Madras Diabetes Research Foundation RCV002052022 SCV002318405 likely pathogenic Neonatal diabetes mellitus criteria provided, single submitter clinical testing

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