ClinVar Miner

List of variants in gene USH2A reported as likely benign for Retinitis pigmentosa-deafness syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_206933.3(USH2A):c.1419C>T (p.Thr473=) rs1805050
NM_206933.3(USH2A):c.2137G>C (p.Gly713Arg) rs696723
NM_206933.3(USH2A):c.3812-8T>G rs646094
NM_206933.3(USH2A):c.4252-36CTTT[5] rs372388546
NM_206933.3(USH2A):c.4627+1038T>C rs439940
NM_206933.3(USH2A):c.4627+1142G>T rs401269
NM_206933.3(USH2A):c.4627+145T>G rs55761862
NM_206933.3(USH2A):c.4627+699C>A rs59704861

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.