ClinVar Miner

Submissions for variant NM_000497.4(CYP11B1):c.800-45C>T

gnomAD frequency: 0.59689  dbSNP: rs7822986
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Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001636216 SCV001851277 benign not provided 2021-05-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001658357 SCV001876475 benign Deficiency of steroid 11-beta-monooxygenase 2021-07-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001636216 SCV005273573 benign not provided criteria provided, single submitter not provided

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