ClinVar Miner

Submissions for variant NM_000497.3(CYP11B1):c.873G>A (p.Ala291=) (rs34570566)

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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 RCV000518376 SCV000613045 benign not specified 2017-07-12 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000380524 SCV000472348 benign Hyperaldosteronism, familial, type I 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000278114 SCV000472349 benign Congenital adrenal hyperplasia 2016-06-14 criteria provided, single submitter clinical testing

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