rs10489629
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0.83x lower risk for spondylitis | |
| (A;G) | 0.83x lower risk for spondylitis | |
| (G;G) | normal risk |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 67222666 |
| Gene | IL23R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10489629 |
| dbSNP (classic) | rs10489629 |
| ClinGen | rs10489629 |
| ebi | rs10489629 |
| HLI | rs10489629 |
| Exac | rs10489629 |
| Gnomad | rs10489629 |
| Varsome | rs10489629 |
| LitVar | rs10489629 |
| Map | rs10489629 |
| PheGenI | rs10489629 |
| Biobank | rs10489629 |
| 1000 genomes | rs10489629 |
| hgdp | rs10489629 |
| ensembl | rs10489629 |
| geneview | rs10489629 |
| scholar | rs10489629 |
| rs10489629 | |
| pharmgkb | rs10489629 |
| gwascentral | rs10489629 |
| openSNP | rs10489629 |
| 23andMe | rs10489629 |
| SNPshot | rs10489629 |
| SNPdbe | rs10489629 |
| MSV3d | rs10489629 |
| GWAS Ctlg | rs10489629 |
| GMAF | 0.4472 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
rs10489629 is one of several SNPs in the IL23R gene that has been shown in a large (over 1,000 Caucasian patients) study to be associated with ankylosing spondylitis. The odds ratio is 0.83 (p=0.00014).[PMID 17952073, PMID 18037607]
[PMID 19034457] Lack of association between interleukin 23 receptor gene polymorphisms and rheumatoid arthritis susceptibility
[PMID 22089529] Associations between interleukin-23R polymorphisms and ankylosing spondylitis susceptibility: a meta-analysis
[PMID 22440928
] Perianal Crohn's Disease: Predictive Factors and Genotype-Phenotype Correlations
[PMID 17068223
] A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.
[PMID 17678723] Investigation of the IL23R gene in a Spanish rheumatoid arthritis cohort.
[PMID 17786191
] rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.
[PMID 18047539] Association between genetic variants in the IL-23R gene and early-onset Crohn's disease: results from a case-control and family-based study among Canadian children.
[PMID 18383363] Association of interleukin-23 receptor variants with ankylosing spondylitis.
[PMID 19175939
] IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease.
[PMID 19306001] No association between interleukin 23 receptor gene polymorphisms and systemic lupus erythematosus.
[PMID 19522770] Variants of the IL23R gene are associated with ankylosing spondylitis but not with Sjogren syndrome in Hungarian population samples.
[PMID 19757086] Interleukin-23 receptor gene variants in Hungarian systemic lupus erythematosus patients.
[PMID 19918037
] Association of interleukin 23 receptor polymorphisms with anti-topoisomerase-I positivity and pulmonary hypertension in systemic sclerosis.
[PMID 20454450
] Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.
[PMID 21253733] Interleukin-23 receptor genetic polymorphisms and ankylosing spondylitis susceptibility: a meta-analysis.
[PMID 22718508] Association of interleukin 23 receptor gene polymorphisms (rs10489629, rs7517847) with rheumatoid arthritis in European population: a meta-analysis.
[PMID 23053963] Associations between interleukin-23 receptor polymorphisms and susceptibility to rheumatoid arthritis: a meta-analysis.
[PMID 28210080
] IL23R single nucleotide polymorphisms could be either beneficial or harmful in ulcerative colitis.
[PMID 27320770] Impact of the IL-17F, IL-23 and IL-23R on susceptibility and phenotype of systemic lupus erythematosus.
- Is a snp
- In dbSNP
- SNPs on chromosome 1
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d
- Pages using PMID magic links
