ClinVar Miner

Submissions for variant NM_001384479.1(AGT):c.1180_1182dup (p.Ala394dup)

dbSNP: rs562507867
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002110308 SCV002432505 likely benign not provided 2024-04-10 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005361974 SCV005920869 uncertain significance Renal tubular dysgenesis of genetic origin 2022-05-06 criteria provided, single submitter research

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