ClinVar Miner

Submissions for variant NM_001242835.2(NDRG4):c.516+4A>G

gnomAD frequency: 0.00352  dbSNP: rs146273834
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 RCV000886399 SCV001029904 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000886399 SCV002008604 likely benign not provided 2021-06-10 criteria provided, single submitter clinical testing

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