ClinVar Miner

Submissions for variant NM_000035.4:c.1_624del

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ATS em Genética Clínica, Universidade Federal do Rio Grande do Sul RCV001376714 SCV001573859 likely pathogenic Hereditary fructosuria 2021-03-18 no assertion criteria provided literature only

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.