List of variants reported as benign for cerebellar degeneration by Mendelics

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_198994.3(TGM6):c.172A>G (p.Met58Val)	rs2076405	0.93204
NM_001378452.1(ITPR1):c.2007G>A (p.Lys669=)	rs2306875	0.68068
NM_173500.4(TTBK2):c.23T>C (p.Leu8Pro)	rs6493068	0.47359
NM_001128164.2(ATXN1):c.772G>T (p.Gly258Cys)	rs144962740
NM_001378452.1(ITPR1):c.4407+44GT[18]	rs35795762
NM_181882.3(PRX):c.4059GGA[6] (p.Glu1361del)	rs139624657
NM_198994.3(TGM6):c.1967+59AG[2]	rs60388755

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.