ClinVar Miner

List of variants reported as likely benign for Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 16
Download table as spreadsheet
NM_015046.7(SETX):c.*2232T>C rs545456048
NM_015046.7(SETX):c.*2506T>C rs73545065
NM_015046.7(SETX):c.*319C>T rs1056912
NM_015046.7(SETX):c.*905A>G rs58327306
NM_015046.7(SETX):c.1693T>C (p.Phe565Leu) rs143982186
NM_015046.7(SETX):c.1880T>C (p.Met627Thr) rs199707503
NM_015046.7(SETX):c.2216G>A (p.Gly739Glu) rs36024203
NM_015046.7(SETX):c.2672T>C (p.Val891Ala) rs148181729
NM_015046.7(SETX):c.3103A>G (p.Lys1035Glu) rs117229601
NM_015046.7(SETX):c.3310C>G (p.Gln1104Glu) rs113831637
NM_015046.7(SETX):c.3992C>T (p.Pro1331Leu) rs11243731
NM_015046.7(SETX):c.4204A>T (p.Thr1402Ser) rs150421712
NM_015046.7(SETX):c.4660T>G (p.Cys1554Gly) rs112089123
NM_015046.7(SETX):c.7640T>C (p.Ile2547Thr) rs151117904
NM_015046.7(SETX):c.7724C>T (p.Pro2575Leu) rs34000644

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.