Skip to main content
. 2016 Mar 25;11(3):e0152476. doi: 10.1371/journal.pone.0152476

Table 1. Associations with celiac disease or tissue transglutaminase autoantibody (tTGA) positivity (p<10−4), mapped to previously known regions.

SNPa CHR BP MAF HR CD P-valueb CD HR tTGA P-valueb tTGA # SNPS (P<10−4) Nearby Gene
rs1936670 1 190598185 0.02 2.23 5.10x10-5 1.36 0.038 1 RGS21
rs4851575 2 102391635 0.24 1.45 5.69x10-5 1.16 0.014 49 IL18R1, IL18RAP
rs114569351 2 68520426 0.02 2.64 4.19x10-5 1.73 0.002 1 PLEK,FBXO48
rs12493471 3 45926682 0.36 1.40 6.36x10-5 1.09 0.098 1 CCR9,LZTFL1,CXCR6
rs1054091 6 159389500 0.17 1.59 5.81x10-6 1.22 0.004 2 RSPH3,TAGAP
rs12990970 2 204408934 0.38 0.82 0.027 0.76 1.26x10-6 21 NPM1P33,CTLA4
rs11709472 3 189560280 0.45 0.82 0.019 0.80 2.75x10-5 8 LPP

CHR: Chromosome; BP: Base Pair Position (NCBI 36.3); MAF: Minor Allele Frequency; HRCD: Hazard Ratio in celiac disease analysis; HRtTGA: Hazard Ratio in tTGA analysis. P-values < 10−4 are highlighted in bold

aThe data for the SNP with smallest p-value is presented from each region.

bHRs and p-value adjusted for family history of celiac disease, HLA-DR-DQ genotype, gender, HLA-DPB1, population stratification (ancestral heterogeneity) and country of residence (as strata).