List of variants in gene MORC2 reported as uncertain significance for Charcot-Marie-Tooth disease

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

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP
NM_001303256.3(MORC2):c.1033G>A (p.Glu345Lys)	rs750686775
NM_001303256.3(MORC2):c.1217C>T (p.Ala406Val)	rs1602485728
NM_001303256.3(MORC2):c.1229T>G (p.Val410Gly)	rs766871664
NM_001303256.3(MORC2):c.158-4A>T	rs763187520
NM_001303256.3(MORC2):c.227-8C>G	rs773796930
NM_001303256.3(MORC2):c.260C>T (p.Ser87Leu)	rs864309504
NM_001303256.3(MORC2):c.707A>G (p.Glu236Gly)	rs886037934
NM_001303256.3(MORC2):c.743A>G (p.Tyr248Cys)	rs1355363942
NM_001303256.3(MORC2):c.754C>T (p.Arg252Trp)	rs864309503

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.