rs909685

This is a regulatory region variant variant in the SYNGR1 gene.

GWAS Catalog Trait Associations (1)

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

rheumatoid arthritis

Allele A
OR 1.13
p 1.0e-16
N 79,799
Large GWAS
multi-ancestry
Allele A
OR 1.11
p 3.0e-9
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 A
OR 0.15
p 4.0e-14
N 2,308
Large GWAS
multi-ancestry

Research that mentions this SNP (1)

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

About SYNGR1

This gene encodes an integral membrane protein associated with presynaptic vesicles in neuronal cells. The exact function of this protein is unclear, but studies of a similar murine protein suggest that it functions in synaptic plasticity without being required for synaptic transmission. The gene product belongs to the synaptogyrin gene family. Three alternatively spliced variants encoding three different isoforms have been identified. [provided by RefSeq, Jul 2008]

View all SYNGR1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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