ClinVar Miner

Submissions for variant NM_001384474.1(LOXHD1):c.1008C>T (p.Gly336=)

gnomAD frequency: 0.00008  dbSNP: rs1444868169
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000982803 SCV001130821 likely benign not provided 2024-05-05 criteria provided, single submitter clinical testing
Natera, Inc. RCV001277112 SCV001463936 uncertain significance Autosomal recessive nonsyndromic hearing loss 77 2020-01-17 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.