functional SNVs variant
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| AA participants | associated_with | functional SNVs | 1e-15 | 1 |
| EA participants | associated_with | functional SNVs | 1e-15 | 1 |
| functional SNVs | associated_with | eQTLGen Consortium | — | 1 |
| functional SNVs | associated_with | gene expression | — | 1 |
Mentioned in (2)
Papers in which this entity is mentioned.
- Annotation of functional variation in personal genomes using RegulomeDB. (2012)
- Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012)
Merged raw entities (2)
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 |
|---|---|---|---|
| functional snvs | variant | 2 | 2 |
| predicted functional snvs | variant | — | — |