ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.1333-1032G>A

gnomAD frequency: 0.01157  dbSNP: rs11821525
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
GeneDx RCV001545443 SCV001764774 likely benign not provided 2018-10-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV001836444 SCV002075817 benign Hereditary hyperinsulinism 2019-10-18 no assertion criteria provided clinical testing

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