Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
0.800 | GeneticVariation | UNIPROT | Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. | 9302278 | 1997 |
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|
0.800 | GeneticVariation | UNIPROT | Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. | 9302278 | 1997 |
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|
0.700 | GeneticVariation | UNIPROT | Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. | 9302278 | 1997 |
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|
0.700 | GeneticVariation | UNIPROT | Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. | 9302278 | 1997 |
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|
0.800 | GeneticVariation | UNIPROT | Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. | 29053796 | 2017 |
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|
0.800 | GeneticVariation | UNIPROT | Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. | 29053796 | 2017 |
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|
0.700 | GeneticVariation | UNIPROT | Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. | 29053796 | 2017 |
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|
0.700 | GeneticVariation | UNIPROT | Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia. | 29053796 | 2017 |
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|
0.800 | GeneticVariation | UNIPROT | Progressive ataxia due to a missense mutation in a calcium-channel gene. | 9345107 | 1997 |
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|
0.800 | GeneticVariation | UNIPROT | Progressive ataxia due to a missense mutation in a calcium-channel gene. | 9345107 | 1997 |
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|
0.700 | GeneticVariation | UNIPROT | Progressive ataxia due to a missense mutation in a calcium-channel gene. | 9345107 | 1997 |
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|
0.700 | GeneticVariation | UNIPROT | Progressive ataxia due to a missense mutation in a calcium-channel gene. | 9345107 | 1997 |