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Iran Red Crescent Med J. 2017 April; 19(4):e44363.doi: 10.5812/ircmj.44363.Published online 2017 February 13.Research ArticlePrevalence of 2 UGT1A1 Gene Variations Related to Gilberts Syndrome in
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01
Get a copy of the genetic testing report for the individual in question
02
Locate the section of the report that discusses the ugt1a1 gene
03
Identify the specific allele being analyzed, in this case prevalence of 2 ugt1a1
04
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01
Healthcare providers who are managing patients with certain medical conditions that may be impacted by variations in the ugt1a1 gene
02
Individuals who are considering certain medications or treatments that are metabolized by the ugt1a1 enzyme
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The prevalence of 2 UGT1A1 refers to the frequency of individuals exhibiting the polymorphism of the UGT1A1 gene that results in reduced enzyme activity, which can lead to increased bilirubin levels.
Individuals or healthcare providers involved in genetic testing, particularly in clinical settings or research, may be required to report the prevalence of 2 UGT1A1.
To fill out prevalence of 2 UGT1A1, you should collect and report genetic test data, demographic information, and any relevant clinical outcomes related to the specific gene polymorphism.
The purpose of reporting the prevalence of 2 UGT1A1 is to monitor genetic risk factors, improve clinical management, facilitate research studies, and inform public health policies.
The information that must be reported includes the number of affected individuals, demographic data, clinical implications, and any relevant population statistics.
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