Research Article

Estimation of the Age of the Kashubian-Specific Pathogenic NPHS2 Variant Responsible for Hereditary Steroid-Resistant Nephrotic Syndrome Points to Its Recent Local Origin

Figure 2

Schematic presentation of the shared haplotypes in the analyzed chromosomes carrying the c.1032delT variant. The maximal length of the inferred ancestral haplotype was ~24 Mb. Frame indicates the core segment of the ancestral haplotype, shared by all the chromosomes carrying c.1032delT mutation.