ClinVar Miner

Submissions for variant NM_018238.4(AGK):c.424-3dup

dbSNP: rs201762775
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
GeneDx RCV001755723 SCV000569330 benign not provided 2021-07-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002063732 SCV002341909 benign Sengers syndrome; Cataract 38 2023-11-25 criteria provided, single submitter clinical testing

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