rs1571878

This is a intron variant variant in the CCR6 gene.

GWAS Catalog Trait Associations (3)

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

rheumatoid arthritis

Allele T
OR 0.86
p 4.0e-40
N 311,292
Meta-analysisLarge GWAS
multi-ancestry
Allele T
OR 1.17
p 5.0e-35
N 79,799
Large GWAS
multi-ancestry
Allele T
OR 1.14
p 5.0e-17
N 55,089
Large GWAS
multi-ancestry
Laufer VA et al. Genetic influences on susceptibility to rheumatoid arthritis in African-Americans. Human Molecular Genetics 28(5):858-874 (2019)
Allele T
OR 0.25
p 1.0e-20
N 2,308
Large GWAS
multi-ancestry

total blood protein measurement

Allele T
OR 0.01
p 1.0e-13
N 394,642
Large GWAS
European

Immunosuppressant use measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.18
p 1.0e-12
N 178,726
Large GWAS
East Asian

Research that mentions this SNP (2)

Reduction of CD83 Expression on B Cells and the Genetic Basis for Rheumatoid Arthritis: Comment on the Article by Thalayasingam et al
FunctionalN=16Yumi Tsuchida et al.(2018)· Arthritis &amp; Rheumatology

This functional study integrates epigenomic datasets (ATAC-seq, Hi-C, ChIP-seq, RNA-seq) from fibroblast-like synoviocytes (FLS) to map the functional relevance of 101 fine-mapped rheumatoid arthritis GWAS associations. FLS regulatory elements account for 24% of RA heritability, and the study assigns putative target genes to RA risk loci, identifying TNFAIP3, IFNAR1, CDK6, RBPJ and others as disease-relevant genes. TNF stimulation reveals dynamic chromatin interactions and differential gene expression at RA-associated regulatory regions.

Traits studied:Rheumatoid arthritis
PLD4 as a novel susceptibility gene for systemic sclerosis in a Japanese population
AssociationN=1,141Chikashi Terao et al.(2013)· Arthritis &amp; Rheumatism

This case-control study identified PLD4 as a novel susceptibility gene for systemic sclerosis (SSc) in a Japanese population, with rs2841277 showing significant association (P=0.00017, OR=1.25). The study also confirmed associations between SSc and rs6932056 in TNFAIP3 (P=0.0000095, OR=1.50) and rs2280381 in IRF8 (P=0.0030, OR=1.26). rs2841280 in PLD4 exon 2 was found in strong linkage disequilibrium with rs2841277 and introduces an amino acid change (E27Q).

Traits studied:Diffuse cutaneous systemic sclerosis (dcSSc)Limited cutaneous systemic sclerosis (lcSSc)Systemic sclerosis

About CCR6

This gene encodes a member of the beta chemokine receptor family, which is predicted to be a seven transmembrane protein similar to G protein-coupled receptors. The gene is preferentially expressed by immature dendritic cells and memory T cells. The ligand of this receptor is macrophage inflammatory protein 3 alpha (MIP-3 alpha). This receptor has been shown to be important for B-lineage maturation and antigen-driven B-cell differentiation, and it may regulate the migration and recruitment of dentritic and T cells during inflammatory and immunological responses. Alternatively spliced transcript variants that encode the same protein have been described for this gene. [provided by RefSeq, Jul 2008]

View all CCR6 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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