Table 1 Minimum common haplotype among 20 FH c.1118A > G carrier families (the variant is highlighted in red). All carriers shared a common 0.61–0.82 Mb haplotype (yellow) delimited by the D1S2785 and D1S2842 microsatellite markers. The minimum common shared haplotype is indicated at the bottom by an arrow

From: Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome