ClinVar Miner

Submissions for variant NM_001384479.1(AGT):c.1096C>T (p.Arg366Trp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005009877 SCV005639191 uncertain significance Renal tubular dysgenesis of genetic origin 2024-05-01 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005009877 SCV005915440 uncertain significance Renal tubular dysgenesis of genetic origin 2022-06-21 criteria provided, single submitter research

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