ClinVar Miner

Submissions for variant NM_000498.3(CYP11B2):c.591A>G (p.Ile197Met) (rs886062744)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000335545 SCV000472519 uncertain significance Corticosterone methyloxidase type 1 deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000395978 SCV000472520 uncertain significance Hyperaldosteronism, familial, type I 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000305481 SCV000472521 uncertain significance Corticosterone methyloxidase type 2 deficiency 2016-06-14 criteria provided, single submitter clinical testing

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