List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 3 by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.2194C>T (p.Pro732Ser)	rs376451611	0.00132
NM_016239.4(MYO15A):c.5060C>T (p.Pro1687Leu)	rs58625281	0.00087
NM_016239.4(MYO15A):c.3659G>A (p.Gly1220Glu)	rs201689819	0.00036
NM_016239.4(MYO15A):c.10394G>A (p.Arg3465Gln)	rs199783506	0.00026
NM_016239.4(MYO15A):c.9620G>A (p.Arg3207His)	rs199621031	0.00026
NM_016239.4(MYO15A):c.5261G>A (p.Arg1754His)	rs544020493	0.00002
NM_016239.4(MYO15A):c.3358C>T (p.Arg1120Cys)	rs375451997
NM_016239.4(MYO15A):c.458A>G (p.Gln153Arg)	rs1597748342
NM_016239.4(MYO15A):c.6550T>C (p.Cys2184Arg)	rs1567649779

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.