ClinVar Miner

Submissions for variant NM_000497.4(CYP11B1):c.596-41C>T

gnomAD frequency: 0.14096  dbSNP: rs113759408
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Human Genetics, Laborarztpraxis Dres. Walther, Weindel und Kollegen RCV001250134 SCV001424541 benign Deficiency of steroid 11-beta-monooxygenase 2020-04-20 criteria provided, single submitter clinical testing
GeneDx RCV001655702 SCV001867810 benign not provided 2021-05-11 criteria provided, single submitter clinical testing

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