ClinVar Miner

Submissions for variant NM_000497.4(CYP11B1):c.425T>A (p.Leu142Ter)

dbSNP: rs1479660166
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV001264087 SCV001442187 likely pathogenic Deficiency of steroid 11-beta-monooxygenase 2019-08-26 criteria provided, single submitter clinical testing

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