ClinVar Miner

Submissions for variant NM_000498.3(CYP11B2):c.1215T>G (p.Val405=)

gnomAD frequency: 0.00006  dbSNP: rs745762132
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
Invitae RCV000917843 SCV001063135 likely benign not provided 2024-01-28 criteria provided, single submitter clinical testing
Natera, Inc. RCV001278109 SCV001465104 uncertain significance Corticosterone methyl oxidase type II deficiency 2020-08-14 no assertion criteria provided clinical testing

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