splice site variants variant
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| splice site variants | associated_with | eQTLGen Consortium | — | 1 |
| splice site variants | associated_with | SNVs | — | 1 |
Mentioned in (2)
Papers in which this entity is mentioned.
- Genetic effects on gene expression across human tissues. (2017)
- Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012)
Merged raw entities (1)
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 |
|---|---|---|---|
| splice site variants | variant | 2 | 2 |