rs4986907, also known as 485G>A, 14269G>A or R162Q, is a SNP in the CYP3A4 gene.

The rs4986907(A) allele defines the CYP3A4*15A variant.

[PMID 17615053] Polymorphisms in the cytochrome P450 genes CYP1A2, CYP1B1, CYP3A4, CYP3A5, CYP11A1, CYP17A1, CYP19A1 and colorectal cancer risk.


Parent Gene: CYP3A4

Importance: 1
Less common allele: T = 0%
More common allele: C = 100%
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