ClinVar Miner

Submissions for variant NM_019885.4(CYP26B1):c.705+7A>G

gnomAD frequency: 0.01395  dbSNP: rs112913461
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 RCV000964865 SCV001112111 benign not provided 2023-11-25 criteria provided, single submitter clinical testing
GeneDx RCV000964865 SCV001818865 likely benign not provided 2019-03-31 criteria provided, single submitter clinical testing

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