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. 2014 Jun 5;26(1):209–219. doi: 10.1681/ASN.2013121339

Figure 1.

Figure 1.

Italian family pedigree. The proband (black arrow) is patient II:1, his wife is II:2, his affected daughter is III:1, and the unaffected son is III:2. Patients II:1 and III:1 are represented as a black square and circle, respectively. The unaffected carrier III:2 is indicated by a black dot. Genotype of CFH single nucleotide polymorphisms targeting the CFH-H3 risk (TGTGT) haplotype (rs3753394 c.1–332 C>T, rs800292 c.184G>A p.V62I, rs1061170 c.1204T>C p.Y402H, rs3753396 c.2016A>G p.Q672Q, and rs1065489 c.2808 G>T p.E936D) and the MCP single nucleotide polymorphism (rs7144 c.*897 T>C) targeting the MCPggaac risk haplotype are reported in red. The age of all subjects is shown. n.a., samples not available. *Chromosome with the duplication.