ClinVar Miner

Submissions for variant NM_000498.3(CYP11B2):c.*292_*294dup

dbSNP: rs3839864
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000378643 SCV000472428 benign Corticosterone 18-monooxygenase deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000284409 SCV000472429 benign Glucocorticoid-remediable aldosteronism 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000320734 SCV000472430 benign Corticosterone methyloxidase type 2 deficiency 2016-06-14 criteria provided, single submitter clinical testing

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