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. 2016 Nov 14;8(12):1455–1469. doi: 10.15252/emmm.201606623

Figure EV2. Haplotype reconstruction for the PAR1 region.

Figure EV2

Pedigree of the family with associated SNPs in the pseudoautosomal region 1 (PAR1) of chromosome X is represented. A total LOD score of 1.7 was identified between the flanking markers rs3995646 and rs5939344 and covered a 2.02 Mb sequence (chrX:706800‐2735491; hg19). Filled symbol, LWD‐affected individual; symbol with a slash, deceased individual; slash, divorced; arrow, index patient. Colored chromosomal regions show traceable inheritance: red color regions, common haplotype co‐segregating with LWD; black lines, regions affected by a crossing over of unknown location.