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. 2020 Apr 20;3:177. doi: 10.1038/s42003-020-0920-6

Table 3.

Validation study for six variants located within six genes previously reported to be associated with Buruli ulcer.

SNP Chr M/m Gene Previous candidate-gene studies GWASa
Study Population MAF Model OR (95% CI) P value MAF OR (95% CI) P valueb
rs1333955 6 C/T PARK2 Capela et al.26 Benin 0.24 Dom 1.43 (1.00–2.06) 0.05 0.27 1.05 (0.64–1.69) 0.357
rs9302752 16 C/T NOD2 Capela et al.26 Benin 0.38 Dom 2.23 (1.14–4.37) 0.02 0.40 1.10 (0.72–1.67) 0.498
rs2241880 2 A/G ATG16L1 Capela et al.26 Benin 0.30 Rec 0.35 (0.13–0.90) 0.02 0.26 0.46 (0.25–0.86) 0.009
rs9282799 17 G/A iNOS Bibert et al.27 Ghana 0.08 Add 1.99 (1.22–3.26) 0.006 0.04 1.33 (0.82–2.14) 0.110
rs2069705 12 A/G IFNG Bibert et al.27 Ghana 0.47 Add 1.56 (1.14–1.99) 0.007 0.43 1.00 (0.82–1.22) 0.482
rs17235409 2 G/A SCL11A1 Stienstra et al.25 Ghana 0.07 Dom 2.50 (1.26–4.96) 0.007 0.09 1.02 (0.20–5.08) 0.257

Chr chromosome, M major allele, m minor allele, MAF minor allele frequency, Dom dominant model, Rec recessive model, Add additive model.

aResults from the GWAS sample obtained with the binary case/control phenotype under the same genetic model as the one used by the corresponding previous study.

bP values for one-tailed tests are given for the marker alleles indicated in bold.