SETX, senataxin, 23064

N. diseases: 133; N. variants: 39
Disease: Cerebellar atrophy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs730882209
rs730882209
Entrez Id: 23064
Gene Symbol: SETX
SETX
CUI: C0740279
Disease:
Cerebellar atrophy 		TC 0.700 GeneticVariation CLINVAR