non-coding variant cohort
Evidence from:
primary |
all sources
Related entities (2)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| non-coding variant | associated_with | complex traits | — | 1 |
| non-coding variant | associated_with | families | — | 1 |
Mentioned in (11)
Papers in which this entity is mentioned.
- Specificity, length and luck drive gene rankings in association studies. (2026)
- Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition. (2025)
- Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
- Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
- Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes. (2018)
- Evaluation of in silico algorithms for use with ACMG/AMP clinical variant interpretation guidelines. (2017)
- A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
- De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
- A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains. (2013)
- The FaceBase Consortium: a comprehensive program to facilitate craniofacial research. (2011)
- Finding the missing heritability of complex diseases. (2009)
Merged raw entities (3)
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 |
|---|---|---|---|
| non-coding variant | variant | 11 | 13 |
| non-coding variant | cohort | — | — |
| non-coding variants | cohort | — | — |