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Informative genomic sequence variants used in fine mapping. Locations of genomic variants where individual I.2 was heterozygous, potentially allowing her disease associated and non-disease associated alleles to be tracked. Sequence variants are illustrated in relation to candidate gene exons (grey boxes) and original microsatellite markers. By chance, all five genes are on the reverse strand of chromosome 5, designated by reverse arrows. rs; as on NCBI dbSNP.
