ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.3399+45C>A

dbSNP: rs200276273
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001589469 SCV001814999 likely benign not provided 2018-09-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001589469 SCV005221364 likely benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV001836458 SCV002075594 benign Hereditary hyperinsulinism 2019-10-18 no assertion criteria provided clinical testing

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