ClinVar Miner

Submissions for variant NM_000685.5(AGTR1):c.761T>A (p.Ile254Asn)

dbSNP: rs2107975615
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV001801269 SCV002047478 uncertain significance Renal tubular dysgenesis of genetic origin 2021-11-02 criteria provided, single submitter clinical testing

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