ClinVar Miner

Submissions for variant NM_000498.3(CYP11B2):c.288T>C (p.Asp96=)

gnomAD frequency: 0.00001  dbSNP: rs751360145
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001518978 SCV001727769 benign not provided 2024-01-24 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832704 SCV002083107 likely benign Corticosterone methyl oxidase type II deficiency 2020-02-28 no assertion criteria provided clinical testing

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