low-frequency variant variant
Evidence from:
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all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| low-frequency variant | associated_with | lung cancer | — | 1 |
Mentioned in (13)
Papers in which this entity is mentioned.
- Advancing regulatory variant effect prediction with AlphaGenome. (2026)
- A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2025)
- Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
- A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2023)
- Transcriptomic signatures across human tissues identify functional rare genetic variation. (2020)
- Quantification of subclonal selection in cancer from bulk sequencing data. (2018)
- Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
- A global reference for human genetic variation. (2015)
- The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
- An integrated map of genetic variation from 1,092 human genomes. (2012)
- Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. (2009)
- Finding the missing heritability of complex diseases. (2009)
- Genome-wide association studies in ADHD. (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 |
|---|---|---|---|
| low frequency variants | variant | 6 | 7 |
| low-frequency variants | variant | 5 | 7 |
| low-frequency variant | variant | 4 | 4 |
| low minor allele frequency variant | variant | — | — |
| maf 0.5%–5% variant | variant | — | — |