ClinVar Miner

Submissions for variant NC_000010.11:g.23259604C>A

gnomAD frequency: 0.00248  dbSNP: rs116846325
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diabetes Molecular Genetics Section, Phoenix Epidemiology and Clinical Research Branch, National Institutes of Health RCV000626378 SCV000608440 benign Type 2 diabetes mellitus no assertion criteria provided case-control

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