ClinVar Miner

Submissions for variant NM_000525.4(KCNJ11):c.754G>T (p.Val252Leu)

dbSNP: rs2133379609
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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 RCV002052019 SCV002318400 likely pathogenic Neonatal diabetes mellitus criteria provided, single submitter clinical testing

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