Source: ALL
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
0.800 | GeneticVariation | UNIPROT | De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. | 29796876 | 2018 |
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|
0.800 | GeneticVariation | UNIPROT | De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. | 30057029 | 2018 |
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|
0.800 | GeneticVariation | UNIPROT | De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. | 29796876 | 2018 |
||||
|
0.800 | GeneticVariation | UNIPROT | De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. | 30057029 | 2018 |
||||
|
0.800 | GeneticVariation | UNIPROT | De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. | 29796876 | 2018 |
||||
|
0.800 | GeneticVariation | UNIPROT | De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. | 30057029 | 2018 |
||||
|
0.800 | GeneticVariation | UNIPROT | High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing. | 27620904 | 2017 |
||||
|
0.800 | GeneticVariation | UNIPROT | High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing. | 27620904 | 2017 |
||||
|
0.800 | GeneticVariation | UNIPROT | High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing. | 27620904 | 2017 |
||||
|
G | 0.800 | CausalMutation | CLINVAR | ||||||
|
C | 0.800 | CausalMutation | CLINVAR | ||||||
|
A | 0.800 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
CA | 0.700 | CausalMutation | CLINVAR | ||||||
|
AC | 0.700 | CausalMutation | CLINVAR |