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[The respective allelic variants, CYP2S1*2 (10347C > T) and CYP2S1*3 (13106C > T; 13255A > G), occurred in our study population at frequencies of 0.50 and 3.75%, respectively. The most common of the variant alleles was CYP2S1*1H (23.8%), harbouring a 13255A > G substitution located in the 3'UTR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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