ClinVar Miner

Submissions for variant NC_000004.12:g.26320917G>A

gnomAD frequency: 0.00141  dbSNP: rs185848565
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV004716515 SCV005298936 benign not provided criteria provided, single submitter not provided
Diabetes Molecular Genetics Section, Phoenix Epidemiology and Clinical Research Branch, National Institutes of Health RCV000626373 SCV000608435 benign Type 2 diabetes mellitus no assertion criteria provided case-control

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