List of variants reported as likely benign for Charcot-Marie-Tooth disease axonal type 2F by Illumina Laboratory Services, Illumina

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_001540.5(HSPB1):c.*22C>T	rs557532119	0.00300
NM_001540.5(HSPB1):c.24C>T (p.Phe8=)	rs201769668	0.00024
NM_001540.5(HSPB1):c.501C>T (p.Ala167=)	rs529095936	0.00007
NM_001540.5(HSPB1):c.-4C>T	rs372833436	0.00005
NM_001540.5(HSPB1):c.383A>G (p.Gln128Arg)	rs558882005	0.00003
NM_001540.5(HSPB1):c.498G>A (p.Glu166=)	rs148357753	0.00002
NM_001540.5(HSPB1):c.108C>G (p.Pro36=)	rs765197724
NM_001540.5(HSPB1):c.365-6C>G	rs200902768

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.