List of variants reported as benign for hereditary sensory and autonomic neuropathy type 5 by Labcorp Genetics (formerly Invitae), Labcorp

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002506.3(NGF):c.104C>T (p.Ala35Val)	rs6330	0.36049
NM_002506.3(NGF):c.54G>A (p.Ala18=)	rs6325	0.04032
NM_002506.3(NGF):c.239G>A (p.Arg80Gln)	rs11466111	0.01173
NM_002506.3(NGF):c.214G>A (p.Val72Met)	rs11466110	0.00727
NM_002506.3(NGF):c.78C>T (p.Val26=)	rs150188752	0.00177
NM_002506.3(NGF):c.191C>T (p.Ala64Val)	rs201087374	0.00011
NM_002506.3(NGF):c.276G>A (p.Gln92=)	rs202060337	0.00006
NM_002506.3(NGF):c.173C>T (p.Ala58Val)	rs201861727	0.00003

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.