List of variants in gene GJB2 reported as likely benign for Deafness, autosomal recessive 1A

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

Total variants: 19

Download table as spreadsheet

HGVS	dbSNP
NM_004004.5(GJB2):c.-216T>G	rs574815423
NM_004004.6(GJB2):c.*1197T>A	rs11841182
NM_004004.6(GJB2):c.*1C>T	rs111033327
NM_004004.6(GJB2):c.*3C>A	rs111033460
NM_004004.6(GJB2):c.-15C>T	rs72561725
NM_004004.6(GJB2):c.108C>T (p.Leu36=)	rs138547875
NM_004004.6(GJB2):c.11G>A (p.Gly4Asp)	rs111033222
NM_004004.6(GJB2):c.120A>C (p.Ala40=)	rs561870637
NM_004004.6(GJB2):c.241C>G (p.Leu81Val)	rs145216882
NM_004004.6(GJB2):c.249C>G (p.Phe83Leu)	rs111033218
NM_004004.6(GJB2):c.312G>A (p.Arg104=)	rs267603770
NM_004004.6(GJB2):c.355G>A (p.Glu119Lys)	rs150529554
NM_004004.6(GJB2):c.368C>A (p.Thr123Asn)	rs111033188
NM_004004.6(GJB2):c.380G>A (p.Arg127His)	rs111033196
NM_004004.6(GJB2):c.456C>T (p.Tyr152=)	rs111033420
NM_004004.6(GJB2):c.457G>A (p.Val153Ile)	rs111033186
NM_004004.6(GJB2):c.478G>A (p.Gly160Ser)	rs34988750
NM_004004.6(GJB2):c.493C>T (p.Arg165Trp)	rs376898963
NM_004004.6(GJB2):c.546G>A (p.Val182=)

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.