Table 2.

Markers analyzed in eight Swedish families (1552, 1894, 19, 765, 1197, 1517, 2143 and F0009520), one Finnish family (9), one French family (10) and three German families (11–13)

The shared disease associated haplotype in the Finnish and Swedish families is highlighted in gray, with the disease allele in underlined bold letters. Other common alleles are illustrated in bold numbers and positions of potential genetic crossover is shown in italic numbers. Physical positions of markers and the mutation in MLH1 according to GRCh37 are indicated at the top of the table