List of variants in gene GPSM2 studied for obsolete rare genetic deafness

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_013296.5(GPSM2):c.1492C>T (p.Arg498Ter)	rs370907055	0.00004
NM_013296.5(GPSM2):c.1063-1G>T	rs773068151	0.00001
NM_013296.5(GPSM2):c.1473del (p.Phe492fs)	rs772372530
NM_013296.5(GPSM2):c.459_460del (p.Ala154fs)	rs727505300
NM_013296.5(GPSM2):c.742del (p.Gly249fs)	rs528069912

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.