haplotype variant
Evidence from:
primary |
all sources
Related entities (13)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| EAGLE consortium | interacts_with | haplotype | — | 1 |
| haplotype | regulates | alcohol sensitivity | — | 1 |
| haplotype | associated_with | case group | — | 1 |
| haplotype | associated_with | cases | — | 1 |
| haplotype | associated_with | control group | — | 1 |
| haplotype | interacts_with | haplotype | — | 1 |
| haplotype | associated_with | heavy drinking | — | 1 |
| haplotype | associated_with | impulsivity | — | 1 |
| haplotype | associated_with | insula | 0.007 | 1 |
| haplotype | associated_with | positive selection | — | 1 |
| haplotype | associated_with | sex | 0.009 | 1 |
| haplotype | associated_with | SNP | — | 1 |
| rare variant | interacts_with | haplotype | — | 1 |
Mentioned in (18)
Papers in which this entity is mentioned.
- Parent-of-origin effects on complex traits in up to 236,781 individuals. (2025)
- Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
- Integrative reconstruction of cancer genome karyotypes using InfoGenomeR. (2021)
- ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing. (2020)
- Genome-wide somatic variant calling using localized colored de Bruijn graphs. (2018)
- Immune diversity sheds light on missing variation in worldwide genetic diversity panels. (2018)
- Ensembl 2017. (2017)
- The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). (2017)
- Fast and accurate long-range phasing in a UK Biobank cohort. (2016)
- Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. (2014)
- GABRA2 markers moderate the subjective effects of alcohol. (2013)
- Impulsiveness and insula activation during reward anticipation are associated with genetic variants in GABRA2 in a family sample enriched for alcoholism. (2012)
- The genetics of the opioid system and specific drug addictions. (2012)
- Meta-analysis and genome-wide interpretation of genetic susceptibility to drug addiction. (2011)
- Statistical analysis strategies for association studies involving rare variants. (2010)
- Expansion of the human mu-opioid receptor gene architecture: novel functional variants. (2009)
- Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sample. (2009)
- FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritization. (2006)
Merged raw entities (4)
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 |
|---|---|---|---|
| haplotype | variant | 18 | 21 |
| composite genomic element | variant | — | — |
| gg haplotype | variant | — | — |
| haplotype pair | variant | — | — |