Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917849
rs121917849
TTPA
0.800 GeneticVariation UNIPROT EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood. 24418350

2014
dbSNP: rs143010236
rs143010236
TTPA
0.800 GeneticVariation UNIPROT EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood. 24418350

2014
dbSNP: rs35916840
rs35916840
TTPA
0.800 GeneticVariation UNIPROT EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood. 24418350

2014
dbSNP: rs397515524
rs397515524
TTPA
0.800 GeneticVariation UNIPROT EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood. 24418350

2014
dbSNP: rs397515526
rs397515526
TTPA
0.800 GeneticVariation UNIPROT EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood. 24418350

2014
dbSNP: rs121917849
rs121917849
TTPA
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010
dbSNP: rs143010236
rs143010236
TTPA
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010
dbSNP: rs35916840
rs35916840
TTPA
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010
dbSNP: rs397515524
rs397515524
TTPA
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010
dbSNP: rs397515526
rs397515526
TTPA
0.800 GeneticVariation UNIPROT EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias. 20050888

2010
dbSNP: rs121917849
rs121917849
TTPA
0.800 GeneticVariation UNIPROT Molecular determinants of heritable vitamin E deficiency. 15065857

2004
dbSNP: rs121917849
rs121917849
TTPA
0.800 GeneticVariation UNIPROT Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families. 15300460

2004
dbSNP: rs121917850
rs121917850
TTPA
0.800 GeneticVariation UNIPROT Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families. 15300460

2004
dbSNP: rs121917850
rs121917850
TTPA
0.800 GeneticVariation UNIPROT Molecular determinants of heritable vitamin E deficiency. 15065857

2004
dbSNP: rs143010236
rs143010236
TTPA
0.800 GeneticVariation UNIPROT Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families. 15300460

2004
dbSNP: rs143010236
rs143010236
TTPA
0.800 GeneticVariation UNIPROT Molecular determinants of heritable vitamin E deficiency. 15065857

2004
dbSNP: rs397515524
rs397515524
TTPA
0.800 GeneticVariation UNIPROT Molecular determinants of heritable vitamin E deficiency. 15065857

2004
dbSNP: rs397515524
rs397515524
TTPA
0.800 GeneticVariation UNIPROT Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families. 15300460

2004
dbSNP: rs397515526
rs397515526
TTPA
0.800 GeneticVariation UNIPROT Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families. 15300460

2004
dbSNP: rs397515526
rs397515526
TTPA
0.800 GeneticVariation UNIPROT Molecular determinants of heritable vitamin E deficiency. 15065857

2004
dbSNP: rs121917849
rs121917849
TTPA
0.800 GeneticVariation UNIPROT Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families. 9463307

1998
dbSNP: rs121917850
rs121917850
TTPA
0.800 GeneticVariation UNIPROT Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families. 9463307

1998
dbSNP: rs143010236
rs143010236
TTPA
0.800 GeneticVariation UNIPROT Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families. 9463307

1998
dbSNP: rs397515524
rs397515524
TTPA
0.800 GeneticVariation UNIPROT Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families. 9463307

1998
dbSNP: rs397515526
rs397515526
TTPA
0.800 GeneticVariation UNIPROT Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families. 9463307

1998