Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606939
rs267606939
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT The frequency of spinocerebellar ataxia type 23 in a UK population. 23108490

2013
dbSNP: rs267606939
rs267606939
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases. 23471613

2013
dbSNP: rs267606940
rs267606940
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT The frequency of spinocerebellar ataxia type 23 in a UK population. 23108490

2013
dbSNP: rs267606940
rs267606940
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases. 23471613

2013
dbSNP: rs267606941
rs267606941
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases. 23471613

2013
dbSNP: rs267606941
rs267606941
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT The frequency of spinocerebellar ataxia type 23 in a UK population. 23108490

2013
dbSNP: rs267606939
rs267606939
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT Perturbations of model membranes induced by pathogenic dynorphin A mutants causing neurodegeneration in human brain. 21712028

2011
dbSNP: rs267606940
rs267606940
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT Perturbations of model membranes induced by pathogenic dynorphin A mutants causing neurodegeneration in human brain. 21712028

2011
dbSNP: rs267606941
rs267606941
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT Perturbations of model membranes induced by pathogenic dynorphin A mutants causing neurodegeneration in human brain. 21712028

2011
dbSNP: rs201486601
rs201486601
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010
dbSNP: rs267606939
rs267606939
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010
dbSNP: rs267606939
rs267606939
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23. 21035104

2010
dbSNP: rs267606940
rs267606940
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23. 21035104

2010
dbSNP: rs267606940
rs267606940
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010
dbSNP: rs267606941
rs267606941
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010
dbSNP: rs267606941
rs267606941
PDYN ; PDYN-AS1
0.800 GeneticVariation UNIPROT Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23. 21035104

2010
dbSNP: rs201486601
rs201486601
PDYN ; PDYN-AS1
A 0.800 CausalMutation CLINVAR

dbSNP: rs267606939
rs267606939
PDYN ; PDYN-AS1
A 0.800 CausalMutation CLINVAR

dbSNP: rs267606940
rs267606940
PDYN ; PDYN-AS1
G 0.800 CausalMutation CLINVAR

dbSNP: rs267606941
rs267606941
PDYN ; PDYN-AS1
A 0.800 GeneticVariation CLINVAR

dbSNP: rs267606941
rs267606941
PDYN ; PDYN-AS1
A 0.800 CausalMutation CLINVAR

dbSNP: rs575606358
rs575606358
PDYN ; PDYN-AS1
0.700 GeneticVariation UNIPROT Identification and characterization of novel PDYN mutations in dominant cerebellar ataxia cases. 23471613

2013
dbSNP: rs575606358
rs575606358
PDYN ; PDYN-AS1
0.700 GeneticVariation UNIPROT The frequency of spinocerebellar ataxia type 23 in a UK population. 23108490

2013
dbSNP: rs575606358
rs575606358
PDYN ; PDYN-AS1
0.700 GeneticVariation UNIPROT Perturbations of model membranes induced by pathogenic dynorphin A mutants causing neurodegeneration in human brain. 21712028

2011
dbSNP: rs575606358
rs575606358
PDYN ; PDYN-AS1
0.700 GeneticVariation UNIPROT Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23. 21035104

2010