ClinVar Miner

Submissions for variant NM_001384474.1(LOXHD1):c.3561G>A (p.Lys1187=)

gnomAD frequency: 0.00024  dbSNP: rs376334860
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
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000215177 SCV000270375 likely benign not specified 2015-04-22 criteria provided, single submitter clinical testing p.Lys1187Lys in Exon 23 of LOXHD1: This variant is not expected to have clinical significance because it does not alter an amino acid residue, is not located wi thin the splice consensus sequence, and has been identified in 4/9450 European c hromosomes by the Exome Aggregation Consortium (ExAC, http://exac.broadinstitute .org; dbSNP rs376334860).
Counsyl RCV000672411 SCV000797512 likely benign Autosomal recessive nonsyndromic hearing loss 77 2018-01-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000943544 SCV001089493 likely benign not provided 2024-11-11 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.