rs2017319 is a SNP in the CYP2C9 gene.

The rs2017319(T) allele defines the CYP2C9_50196C>T variant, about which little is known.

[PMID 18698231] Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.

rs2017319

Parent Gene: CYP2C9

Importance: 1
Less common allele: T = 3%
More common allele: C = 97%
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