Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10865331
rs10865331
0.870 GeneticVariation BEFREE This is the first study that replicates in an independent cohort the association of the intergenic SNP rs10865331 with susceptibility to AS. 20810504

2010

dbSNP: rs10865331
rs10865331
A 0.870 GeneticVariation GWASDB Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. 20062062

2010

dbSNP: rs10865331
rs10865331
0.870 GeneticVariation BEFREE Association was also observed between AS and the intergenic region 2p15 (rs10865331, p = 0.023). 21068102

2011

dbSNP: rs10865331
rs10865331
A 0.870 GeneticVariation GWASCAT Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. 20062062

2010

dbSNP: rs10865331
rs10865331
0.870 GeneticVariation BEFREE Beyond that, we also demonstrated a strong relationship between rs10865331 and AS susceptibility (OR (95% CI) = 1.303(1.111-1.526)). 28493913

2017

dbSNP: rs10865331
rs10865331
A 0.870 GeneticVariation GWASDB Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. 21743469

2011

dbSNP: rs10865331
rs10865331
0.870 GeneticVariation BEFREE Through logistic regression, we built the AS-GRS model consisting of 5 genetic components: HLA-B27, 3 CNV (1q32.2, 13q13.1, and 16p13.3), and 1 SNP (rs10865331). 27909141

2016

dbSNP: rs10865331
rs10865331
0.870 GeneticVariation BEFREE We found that rs10865331 was significantly associated with AS susceptibility and with Bath AS Function Index (BASFI). 25184745

2014

dbSNP: rs10865331
rs10865331
0.870 GeneticVariation BEFREE We revealed 16 AS-associated variants with nominal evidence in Han Chinese, including rs10865331 (P=6.30×10-10), rs10050860 (P=4.09×10-5) and rs8070463 (P=1.03×10-4). 31523044

2019

dbSNP: rs10865331
rs10865331
0.870 GeneticVariation BEFREE This is the first confirmation in a nonwhite population that genetic polymorphisms of rs27037, rs27434, and rs10865331 are associated with AS, implicating common pathogenetic mechanisms in Korean and white patients with AS. 21041274

2011

dbSNP: rs10865331
rs10865331
A 0.870 GeneticVariation GWASCAT Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. 21743469

2011

dbSNP: rs8070463
rs8070463
0.820 GeneticVariation BEFREE We revealed 16 AS-associated variants with nominal evidence in Han Chinese, including rs10865331 (P=6.30×10-10), rs10050860 (P=4.09×10-5) and rs8070463 (P=1.03×10-4). 31523044

2019

dbSNP: rs8070463
rs8070463
C 0.820 GeneticVariation GWASCAT Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. 21743469

2011

dbSNP: rs8070463
rs8070463
C 0.820 GeneticVariation GWASDB Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. 21743469

2011

dbSNP: rs8070463
rs8070463
0.820 GeneticVariation BEFREE The rs7379457 SNP in PPARGC1B, the rs1395621 and rs9438876 SNPs in RUNX3, and the rs8070463 SNP in TBKBP1 are related to the severity of AS in Chinese Han population. 23637848

2013

dbSNP: rs10440635
rs10440635
A 0.810 GeneticVariation GWASCAT Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. 21743469

2011

dbSNP: rs10440635
rs10440635
0.810 GeneticVariation BEFREE The rs11062357 SNP in JARID1A, the rs2607142 SNP in JMY and rs10440635 in PTGER4 are related to severity of AS. 24069348

2013

dbSNP: rs10440635
rs10440635
A 0.810 GeneticVariation GWASDB Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. 21743469

2011

dbSNP: rs2242944
rs2242944
0.810 GeneticVariation BEFREE A recent genome-wide association study has identified 2 single-nucleotide polymorphisms (SNP) associated with ankylosing spondylitis (AS), rs10865331 (2p15) and rs2242944 (21q22). 20810504

2010

dbSNP: rs2242944
rs2242944
A 0.810 GeneticVariation GWASDB Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. 20062062

2010

dbSNP: rs2242944
rs2242944
0.810 GeneticVariation GWASCAT Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. 20062062

2010

dbSNP: rs2310173
rs2310173
A 0.810 GeneticVariation GWASDB Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. 20062062

2010

dbSNP: rs2310173
rs2310173
0.810 GeneticVariation BEFREE However, we observed that CARD9 allele C (p = 0.012) and genotype CC (p = 0.012) were significant protective factors against AS only in HLA-B27-negative patients, and IL1R2 rs2310173 genotype GT was mildly protective against AS only in HLA-B27-negative status. 26590821

2016

dbSNP: rs2310173
rs2310173
A 0.810 GeneticVariation GWASCAT Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. 20062062

2010

dbSNP: rs4552569
rs4552569
0.810 GeneticVariation BEFREE The correlation between genetic polymorphisms, AS activity indexes, (namely, BASDAI, BASFI and BAS-G) and AS complications (uveitis and inflammatory bowel disease) were tested using the markers, rs4552569 and rs17095830. 23308121

2013