ClinVar Miner

Submissions for variant NM_000498.3(CYP11B2):c.1398+4A>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005041022 SCV005675172 uncertain significance Corticosterone 18-monooxygenase deficiency; Corticosterone methyloxidase type 2 deficiency 2024-02-11 criteria provided, single submitter clinical testing

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