|| CYP3A4*3 homozygote
|| carrier of one CYP3A4*3 allele
|?|| (C;C) (C;T) (T;T) ||28|
, also known as 1334T>C, 23171T>C or M445T, is a SNP in the CYP3A4
The rs4986910(C) allele defines the CYP3A4*3 variant.
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[PMID 17615053] Polymorphisms in the cytochrome P450 genes CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1, CYP19A1 and colorectal cancer risk.
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