1q21.1 deletion variant
Evidence from:
primary |
all sources
Related entities (6)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| 1q21.1 deletion | associated_with | autism | — | 1 |
| 1q21.1 deletion | associated_with | epilepsy | — | 1 |
| 1q21.1 deletion | associated_with | head size | — | 1 |
| 1q21.1 deletion | associated_with | mental retardation | — | 1 |
| 1q21.1 deletion | associated_with | psychiatric traits | — | 1 |
| 1q21.1 deletion | risk_factor_for | schizophrenia | — | 1 |
Mentioned in (3)
Papers in which this entity is mentioned.
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- A syndrome of short stature, microcephaly and speech delay is associated with duplications reciprocal to the common Sotos syndrome deletion. (2010)
- Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
Merged raw entities (5)
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 |
|---|---|---|---|
| 1q21.1 deletion | variant | 3 | 8 |
| 1q21.1 cnv deletion | variant | — | — |
| 1q21.1 del | variant | — | — |
| 1q21.1 microdeletion | variant | — | — |
| deletions at chr1q21.1 | variant | — | — |