Figure 2
From: Genome-wide linkage and exome analyses identify variants of HMCN1for splenic epidermoid cyst
Pedigree of a Japanese family with splenic epidermoid cyst and co-segregation of R5205H variant of HMCN1 . Filled squares and circles denote affected individuals and open symbols represent unaffected subjects. The arrow indicates the proband (IV:3). The genotypes are for the R5205H variant of HMCN1, which is co-segregating with the affection status except for III-3, III-4, and IV-1.