ClinVar Miner

Submissions for variant NM_024884.3(L2HGDH):c.1174A>G (p.Ile392Val)

gnomAD frequency: 0.00009  dbSNP: rs373172891
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000503896 SCV000595492 uncertain significance not specified 2017-01-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000882412 SCV001025651 likely benign L-2-hydroxyglutaric aciduria 2024-12-29 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003942637 SCV004757712 likely benign L2HGDH-related disorder 2022-12-02 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.