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. Author manuscript; available in PMC: 2023 Oct 30.
Published in final edited form as: J Autoimmun. 2022 Aug 18;132:102882. doi: 10.1016/j.jaut.2022.102882

Fig. 1.

Fig. 1.

(A) A Manhattan plot showing the results of the case-case genetic association analysis of male and female patients with Behcet’s disease of Turkish origin. The −Log10(P) value for each variant is plotted against its chromosomal position. The red line represents the genome-wide level of significance (P < 5 × 10−8) and the blue line represents the suggestive level of significance (P < 1 × 10−5). (B) Regional plot displaying SNPs in LD with rs2848712 in the HLA region in the Turkish population (LD = 1 is blue, LD = 0.99–0.80 is red, LD = 0.79–0.60 is orange, LD = 0.59–0.40 is green, and LD = 0.39–0.00 is black). The −Log10(P) value for each variant is plotted against its physical position on chromosome 6. The red line represents GWAS level of significance (P < 5 × 10−8) and the blue line represents suggestive level of significance (P < 1 × 10−5). (Assembly_GRCh37/hg19 by Ensembl was used).