LGD variant
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| LGD | risk_factor_for | ASD | — | 1 |
| LGD | risk_factor_for | OCD | — | 1 |
| LGD | associated_with | risk genes | — | 1 |
| LGD | risk_factor_for | TD | — | 1 |
Mentioned in (5)
Papers in which this entity is mentioned.
- Specificity, length and luck drive gene rankings in association studies. (2026)
- Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
- De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
- Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
Merged raw entities (4)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| lgd | variant | 3 | 3 |
| loss-of-function | variant | 2 | 2 |
| de novo lgd | variant | 1 | 3 |
| likely gene disrupting | variant | — | — |