List of variants in gene GJB2 reported as uncertain significance for Hearing loss

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

Download table as spreadsheet

HGVS	dbSNP
NM_004004.6(GJB2):c.101T>C (p.Met34Thr)	rs35887622
NM_004004.6(GJB2):c.226C>G (p.Leu76Val)	rs1566528748
NM_004004.6(GJB2):c.355G>A (p.Glu119Lys)	rs150529554
NM_004004.6(GJB2):c.560A>G (p.Glu187Gly)	rs1451982228

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.