ClinVar Miner

Submissions for variant NM_019885.4(CYP26B1):c.51G>A (p.Ala17=)

gnomAD frequency: 0.00099  dbSNP: rs368056183
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 RCV000954880 SCV001101546 benign not provided 2023-12-22 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000954880 SCV004811126 likely benign not provided 2024-03-01 criteria provided, single submitter clinical testing CYP26B1: BP4, BP7

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