ClinVar Miner

Submissions for variant NM_000497.4(CYP11B1):c.396-9C>T

gnomAD frequency: 0.00001  dbSNP: rs1324660372
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002205811 SCV002363293 likely benign not provided 2023-05-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494130 SCV002801832 likely benign Deficiency of steroid 11-beta-monooxygenase; Glucocorticoid-remediable aldosteronism 2022-02-09 criteria provided, single submitter clinical testing

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