{{Rsnum
|rsid=11039155
|Gene=NR1H3
|Chromosome=11
|position=47259211
|Orientation=plus
|GMAF=0.07851
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=NR1H3
}}NR1H3 gene SNP associated with [[metabolic syndrome]] and thus potentially [[type-2 diabetes]] and [[heart disease]].{{PMID|18209740}}

{{PMID Auto
|PMID=19041386
|Title=Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.
|OA=1
}}

{{PMID Auto
|PMID=19292929
|Title=Functional and genetic analysis in type 2 diabetes of liver X receptor alleles--a cohort study.
|OA=1
}}

{{PMID Auto
|PMID=21316679
|Title=Associations between common genetic polymorphisms in the liver X receptor alpha and its target genes with the serum HDL-cholesterol concentration in adolescents of the HELENA Study.
}}

{{PMID Auto
|PMID=22311022
|Title=Genetic variations in SREBP-1 and LXRalpha are not directly associated to PCOS but contribute to the physiological specifics of the syndrome.
}}

{{PMID Auto
|PMID=24100084
|Title=Lack of association between LXRα and LXRβ gene polymorphisms and prevalence of metabolic syndrome: a case-control study of an Iranian population
}}

{{PMID Auto
|PMID=25005769
|Title=Association Between Single Nucleotide Polymorphisms of Sterol Regulatory Element Binding Protein-2 and Liver X Receptor α Gene and Risk of Polycystic Ovary Syndrome in a Chinese Han Population
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}