ClinVar Miner

Submissions for variant NM_003383.5(VLDLR):c.1245C>T (p.Gly415=)

gnomAD frequency: 0.00003  dbSNP: rs746308049
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 RCV000902881 SCV001047322 likely benign not provided 2024-06-17 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818756 SCV002071613 uncertain significance not specified 2017-11-08 criteria provided, single submitter clinical testing

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