List of variants reported as benign for autosomal dominant nonsyndromic hearing loss 9

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

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004086.3(COCH):c.1055C>G (p.Thr352Ser)	rs1045644	0.51720
NM_004086.3(COCH):c.*27A>T	rs13122	0.24742
NM_004086.3(COCH):c.1477+9C>A	rs17097458	0.05034
NM_004086.3(COCH):c.*407C>T	rs7152503	0.02116
NM_004086.3(COCH):c.1269C>T (p.Asp423=)	rs35353967	0.00689
NM_004086.3(COCH):c.1553A>G (p.Glu518Gly)	rs17097468	0.00602
NM_004086.3(COCH):c.1026C>T (p.Tyr342=)	rs28362777	0.00173
NM_004086.3(COCH):c.630-9T>C	rs368182881	0.00002
NM_004086.3(COCH):c.*39G>T	rs555882283	0.00001
NM_004086.3(COCH):c.239+5G>A	rs563163157	0.00001

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.