rs2279238
| Orientation | minus |
| Stabilized | minus |
| Make rs2279238(A;A) |
| Make rs2279238(A;G) |
| Make rs2279238(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 47260473 |
| Gene | NR1H3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2279238 |
| dbSNP (classic) | rs2279238 |
| ClinGen | rs2279238 |
| ebi | rs2279238 |
| HLI | rs2279238 |
| Exac | rs2279238 |
| Gnomad | rs2279238 |
| Varsome | rs2279238 |
| LitVar | rs2279238 |
| Map | rs2279238 |
| PheGenI | rs2279238 |
| Biobank | rs2279238 |
| 1000 genomes | rs2279238 |
| hgdp | rs2279238 |
| ensembl | rs2279238 |
| geneview | rs2279238 |
| scholar | rs2279238 |
| rs2279238 | |
| pharmgkb | rs2279238 |
| gwascentral | rs2279238 |
| openSNP | rs2279238 |
| 23andMe | rs2279238 |
| SNPshot | rs2279238 |
| SNPdbe | rs2279238 |
| MSV3d | rs2279238 |
| GWAS Ctlg | rs2279238 |
| GMAF | 0.348 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22029530
] A common polymorphism in NR1H2 (LXRbeta) is associated with preeclampsia
[PMID 17108812] Liver X receptor gene polymorphisms and adipose tissue expression levels in obesity.
[PMID 19292929] Functional and genetic analysis in type 2 diabetes of liver X receptor alleles--a cohort study.
[PMID 21042792] Genetic variation within the NR1H2 gene encoding liver X receptor beta associates with insulin secretion in subjects at increased risk for type 2 diabetes.
[PMID 21562465] Liver X receptor alpha gene polymorphisms and variable cardiovascular outcomes in patients treated with antihypertensive therapy: results from the INVEST-GENES study.
[PMID 22311022] Genetic variations in SREBP-1 and LXRalpha are not directly associated to PCOS but contribute to the physiological specifics of the syndrome.
[PMID 24100084] Lack of association between LXRα and LXRβ gene polymorphisms and prevalence of metabolic syndrome: a case-control study of an Iranian population
[PMID 24788534] Liver X Receptor Gene Polymorphisms in Tuberculosis: Effect on Susceptibility
[PMID 28244008] Liver X Receptor Genes Variants Modulate ALS Phenotype.
