ClinVar Miner

Submissions for variant NM_130849.4(SLC39A4):c.1141A>G (p.Thr381Ala)

gnomAD frequency: 0.04681  dbSNP: rs75920625
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000296860 SCV000472564 likely benign Hereditary acrodermatitis enteropathica 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001520475 SCV001729580 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001520475 SCV005222384 likely benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV000296860 SCV002083118 benign Hereditary acrodermatitis enteropathica 2019-11-27 no assertion criteria provided 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.