Source: ALL
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
0.700 | GeneticVariation | UNIPROT | A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation. | 25114083 | 2015 |
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|
0.700 | GeneticVariation | UNIPROT | Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. | 24899140 | 2014 |
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|
0.700 | GeneticVariation | UNIPROT | SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis. | 24042580 | 2013 |
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|
0.700 | GeneticVariation | UNIPROT | SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis. | 22084127 | 2011 |