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A DNA variant has been found linked to a rare autosomal dominant disease in humans and can thus be used as a marker to follow inheritance of the disease allele. In an informative family (in which one parent is heterozygous for both the disease allele and the DNA marker in a known chromosomal arrangement of alleles, and his or her mate does not have the same alleles of the DNA variant), the reliability of such a marker as a predictor of the disease in a fetus is related to the map distance betwee
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