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. 2011 Dec 8;21(6):1336–1349. doi: 10.1093/hmg/ddr572

Figure 1.

Figure 1.

Pedigree analysis of the GLC1F family and disease haplotype. Black symbols denote patients with POAG, and white symbols denote unaffected or unknown status. Genotypes are listed in the order given by the map to the left. The haplotype of the disease chromosome is boxed. Both SNPs that determined the linkage interval (rs4401760 in II-1 and rs73161885 in IV-2 and IV-3) are also shown. The synonymous mutation in ASB10 found in the family is indicated by Thr255Thr (c.765C>T). Note that the T allele of Thr255Thr segregates with the disease haplotype.