ClinVar Miner

Submissions for variant NM_000500.9(CYP21A2):c.1439G>T (p.Arg480Leu) (rs184649564)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000514693 SCV000841734 uncertain significance not provided 2018-05-18 criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000514693 SCV000610624 benign not provided 2017-05-02 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000514693 SCV000700353 uncertain significance not provided 2017-02-16 criteria provided, single submitter clinical testing

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