List of variants reported as uncertain significance for Charcot-Marie-Tooth disease axonal type 2K; Charcot-Marie-Tooth disease type 4A; Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive; Charcot-Marie-Tooth disease recessive intermediate A

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: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_018972.4(GDAP1):c.556A>G (p.Ile186Val)	rs148508128	0.00040
NM_018972.4(GDAP1):c.1006G>T (p.Ala336Ser)	rs140811185	0.00007
NM_018972.4(GDAP1):c.721G>A (p.Gly241Ser)	rs533081002	0.00003
NM_018972.4(GDAP1):c.347T>C (p.Met116Thr)	rs281865060

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.