List of variants reported as benign for cerebellar disorder by Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital

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_001382391.1(CSPP1):c.2539-12T>A	rs185726462	0.00080
NM_001372574.1(ATXN2):c.59AGC[8] (p.Gln28del)	rs10560189
NM_001382391.1(CSPP1):c.2392-8_2392-4del	rs528357182
NM_020247.4(COQ8A):c.807_808insT	rs3215920

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.