ClinVar Miner

Submissions for variant NM_001382817.3(AGT):c.-30-3287A>C

dbSNP: rs5050
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000377471 SCV000355410 likely benign Renal tubular dysgenesis 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001651344 SCV001861843 benign not provided 2019-04-18 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 30383794, 9403548, 22216295, 9931090, 19021695, 18802024)
Breakthrough Genomics, Breakthrough Genomics RCV001651344 SCV005264347 likely benign not provided criteria provided, single submitter not provided

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