Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs151344517
rs151344517
AFG3L2 ; TUBB6 ; LOC107985154
T 0.700 CausalMutation CLINVAR Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias. 20725928

2010
dbSNP: rs138308105
rs138308105
CLDN16
A 0.700 CausalMutation CLINVAR

dbSNP: rs1441937959
rs1441937959
EFL1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557551678
rs1557551678
CLDN19
A 0.700 CausalMutation CLINVAR

dbSNP: rs1563452941
rs1563452941
SLC20A2
A 0.700 CausalMutation CLINVAR