ClinVar Miner

Submissions for variant NM_000340.2(SLC2A2):c.469G>C (p.Gly157Arg)

dbSNP: rs750836049
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Cyto-molecular Genetics, Department of Anatomy, All India Institute of Medical Sciences (AIIMS), New Delhi RCV001843686 SCV002102791 likely pathogenic Fanconi-Bickel syndrome 2022-03-07 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001843686 SCV003825668 uncertain significance Fanconi-Bickel syndrome 2021-06-22 criteria provided, single submitter clinical testing

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.