nsSNP variant
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| HLA | associated_with | nsSNP | — | 1 |
| nsSNP | associated_with | case cohort | — | 1 |
| nsSNP | associated_with | control | — | 1 |
| nsSNP | associated_with | dbSNP | — | 1 |
Mentioned in (7)
Papers in which this entity is mentioned.
- Human Genetics of Addiction: New Insights and Future Directions. (2018)
- Candidate gene association studies: a comprehensive guide to useful in silico tools. (2013)
- A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. (2013)
- Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
- Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations. (2009)
- Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. (2007)
- SNPs3D: candidate gene and SNP selection for association studies. (2006)
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 |
|---|---|---|---|
| nssnp | variant | 5 | 5 |
| missense snp | variant | 2 | 2 |