rs7429279

This is a intron variant variant in the RARB gene.

GWAS Catalog Trait Associations (3)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

taste liking measurement

Allele C
OR 0.03
p 1.0e-12
N 159,527
Large GWAS
European

dentures

Allele A
OR 0.04
p 5.0e-10
N 461,031
Large GWAS
European

dental caries, dentures

Allele A
OR 0.02
p 1.0e-9
N 487,823
Large GWAS
multi-ancestry

About RARB

This gene encodes retinoic acid receptor beta, a member of the thyroid-steroid hormone receptor superfamily of nuclear transcriptional regulators. This receptor localizes to the cytoplasm and to subnuclear compartments. It binds retinoic acid, the biologically active form of vitamin A which mediates cellular signalling in embryonic morphogenesis, cell growth and differentiation. It is thought that this protein limits growth of many cell types by regulating gene expression. The gene was first identified in a hepatocellular carcinoma where it flanks a hepatitis B virus integration site. Alternate promoter usage and differential splicing result in multiple transcript variants. [provided by RefSeq, Mar 2014]

View all RARB variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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