Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908215
rs121908215
T 0.800 CausalMutation CLINVAR

dbSNP: rs121908217
rs121908217
T 0.800 CausalMutation CLINVAR

dbSNP: rs1057520918
rs1057520918
T 0.700 CausalMutation CLINVAR

dbSNP: rs121908212
rs121908212
A 0.700 CausalMutation CLINVAR

dbSNP: rs121909324
rs121909324
A 0.700 CausalMutation CLINVAR

dbSNP: rs121909326
rs121909326
G 0.700 CausalMutation CLINVAR

dbSNP: rs794727411
rs794727411
T 0.700 GeneticVariation CLINVAR

dbSNP: rs863224852
rs863224852
T 0.700 GeneticVariation CLINVAR

dbSNP: rs886037945
rs886037945
T 0.700 CausalMutation CLINVAR

dbSNP: rs121908215
rs121908215
0.800 GeneticVariation UNIPROT A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation. 20682717

2010

dbSNP: rs121908217
rs121908217
0.800 GeneticVariation UNIPROT A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation. 20682717

2010

dbSNP: rs121908245
rs121908245
0.700 GeneticVariation UNIPROT A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation. 20682717

2010

dbSNP: rs121908247
rs121908247
0.700 GeneticVariation UNIPROT A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation. 20682717

2010

dbSNP: rs121908215
rs121908215
0.800 GeneticVariation UNIPROT Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. 8988170

1997

dbSNP: rs121908217
rs121908217
0.800 GeneticVariation UNIPROT Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. 8988170

1997

dbSNP: rs121908245
rs121908245
0.700 GeneticVariation UNIPROT Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. 8988170

1997

dbSNP: rs121908247
rs121908247
0.700 GeneticVariation UNIPROT Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. 8988170

1997

dbSNP: rs121908215
rs121908215
0.800 GeneticVariation UNIPROT Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. 16325861

2006

dbSNP: rs121908217
rs121908217
0.800 GeneticVariation UNIPROT Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. 16325861

2006

dbSNP: rs121908245
rs121908245
0.700 GeneticVariation UNIPROT Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. 16325861

2006

dbSNP: rs121908247
rs121908247
0.700 GeneticVariation UNIPROT Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. 16325861

2006

dbSNP: rs121908215
rs121908215
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010

dbSNP: rs121908217
rs121908217
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010

dbSNP: rs121908215
rs121908215
0.800 GeneticVariation UNIPROT EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood. 24418350

2014

dbSNP: rs121908217
rs121908217
0.800 GeneticVariation UNIPROT EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood. 24418350

2014