List of variants reported as pathogenic for cerebellar disorder by Institute of Human Genetics, Cologne University

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: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000144.5(FXN):c.438C>G (p.Asn146Lys)	rs146818694
NM_014363.6(SACS):c.2903_2906del (p.Asp968fs)	rs1259615333
NM_015046.7(SETX):c.5308_5311del (p.Glu1770fs)	rs750959420
NM_015378.4(VPS13D):c.12350C>G (p.Ser4117Ter)	rs1645321968
NM_182961.4(SYNE1):c.20970del (p.Asp6991fs)	rs1554247806

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.