rare variation cohort
Evidence from:
primary |
all sources
Related entities (13)
Mentioned in (8)
Papers in which this entity is mentioned.
- The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. (2022)
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
- A global reference for human genetic variation. (2015)
- A global reference for human genetic variation. (2015)
- Guidelines for investigating causality of sequence variants in human disease. (2014)
- Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
- Common biological networks underlie genetic risk for alcoholism in African- and European-American populations. (2013)
- Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012)
Merged raw entities (7)
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 |
|---|---|---|---|
| rare variation | variant | 8 | 12 |
| excess of rare variation | cohort | — | — |
| rare genetic variation | cohort | — | — |
| rarer variation | cohort | — | — |
| rare snv | cohort | — | — |
| rare snvs | cohort | — | — |
| rare variation | cohort | — | — |