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- W2801216977 abstract "The human DNA sequence is highly polymorphic; for a typical gene, different people have different specific sequences (or alleles) for that gene. As a result, for the typical protein, different people have different levels of activity in that protein. If the activity of a protein is significantly greater or less than the level of activity that is seen in the typical person, that individual will have a greater or lesser susceptibility to the diseases the protein’s function influences than the typical person does. Whether a high-activity or low-activity gene allele represents a risk-increasing allele or a risk-decreasing allele depends on the specific function the protein performs. While some risk-increasing alleles are relatively common, and some increase the individual’s risk for the associated disease dramatically, most risk-increasing alleles are relatively rare, and most only increase the individual’s risk for the associated disease by a small amount." @default.
- W2801216977 created "2018-05-17" @default.
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- W2801216977 date "2018-01-01" @default.
- W2801216977 modified "2023-09-23" @default.
- W2801216977 title "Review of Clinical Human Medical Genetics" @default.
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- W2801216977 doi "https://doi.org/10.1016/b978-0-12-814610-1.00003-1" @default.
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