Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2227982
rs2227982
PDCD1 ; LOC105373977
0.040 GeneticVariation BEFREE Our results showed that SNPs rs2227982 and rs10204525 were interrelated to AAU; the influence on AAU could be related with gender, HLA-B27, and AS stat</span>us. 30540488

2019
dbSNP: rs2227982
rs2227982
PDCD1 ; LOC105373977
0.040 GeneticVariation BEFREE Our meta-analysis demonstrated that the rs2227982 polymorphism in the PD-1 gene might contribute to AS susceptibility. 26232179

2016
dbSNP: rs2227982
rs2227982
PDCD1 ; LOC105373977
0.040 GeneticVariation BEFREE Our study confirms a significant association between the SNP rs2227982 of PDCD-1 gene and the susceptibility of AS in a Chinese Han population. 23620109

2013
dbSNP: rs2227982
rs2227982
PDCD1 ; LOC105373977
0.040 GeneticVariation BEFREE The frequency of the CT haplotype (PD-1 rs2227981 C allele and PD-1 rs2227982 T allele) was higher in the AS patient group comparing with the controls (odds ratio (OR)=1.845, 95% confidence interval 1.220-2.789). 21269571

2011