Figure 4.

Scatter plots showing the results from genotyping a panel of variant nucleotides in the factor V and the HLA-H genes. The SNPs from the FV gene had been selected from those described by Cargill et al. (1999). The polymorphism WIAF-10964 lies in exon 10 as the FVLeidenmutation (Bertina et al. 1994), while the other SNPs are located in exon 13 of the gene. The polymorphism IVS2 lies in intron 2 (Beutler et al. 1997), the HHC282Y mutation in exon 4 (Feder et al. 1996) and 5569A/G in intron 4 (Jeffrey et al. 1999) of the HLA-H gene. The six FV and two HLA-H gene SNPs, along with FVLeiden and HHC282Y mutations, were analyzed in 53 known FVLeiden mutation and in 84 known HHC282Y mutation carriers or homozygotes, and in 94 individuals known to be of normal genotype at both the mutant sites. The signal intensity ratios are given on the y-axis and the signal intensities on thex-axis.

6f4_L4TT