ClinVar Miner

List of variants reported as benign for Autosomal recessive nonsyndromic hearing loss 84B by Genome-Nilou Lab

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001378609.3(OTOGL):c.2519-31A>G rs4483657 0.71868
NM_001378609.3(OTOGL):c.6429G>A (p.Glu2143=) rs777315488 0.00001
NM_001378609.3(OTOGL):c.3702G>A (p.Met1234Ile) rs1207446497
NM_001378609.3(OTOGL):c.5067T>C (p.Asp1689=) rs1888797330
NM_001378609.3(OTOGL):c.5957G>A (p.Arg1986Lys) rs1440977583

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.