Source: ALL
| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
0.800 | GeneticVariation | UNIPROT | Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder. | 26647308 | 2016 |
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|
A | 0.800 | CausalMutation | CLINVAR | Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder. | 26647308 | 2016 |
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|
0.800 | GeneticVariation | UNIPROT | De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment. | 20950788 | 2010 |