noncoding variant variant
Evidence from:
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all sources
Related entities (5)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| indel | associated_with | noncoding variant | — | 1 |
| noncoding variant | risk_factor_for | alcoholism risk | — | 1 |
| noncoding variant | regulates | gene expression | — | 1 |
| SNV | associated_with | noncoding variant | — | 1 |
| structural variant | associated_with | noncoding variant | — | 1 |
Mentioned in (11)
Papers in which this entity is mentioned.
- Genome modelling and design across all domains of life with Evo 2. (2026)
- Functional analysis of cancer-associated germline risk variants. (2025)
- Multiple overlapping binding sites determine transcription factor occupancy. (2025)
- Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
- The impact of structural variation on human gene expression. (2017)
- Somatic cancer variant curation and harmonization through consensus minimum variant level data. (2016)
- Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
- ACMG clinical laboratory standards for next-generation sequencing. (2013)
- Annotation of functional variation in personal genomes using RegulomeDB. (2012)
- The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)
- The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)
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 |
|---|---|---|---|
| noncoding variant | variant | 9 | 11 |
| noncoding variants | variant | 4 | 4 |
| regulomedb-predicted variants | variant | — | — |