SNX14, sorting nexin 14, 57231

N. diseases: 59; N. variants: 12
Disease: Cerebellar atrophy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201128942
rs201128942
Entrez Id: 57231
Gene Symbol: SNX14
SNX14
CUI: C0740279
Disease:
Cerebellar atrophy 		T 0.700 CausalMutation CLINVAR