rs1713449 was positively associated with the risk of male infertility (OR=1.39; Ptrend<0.001) [R].

The allele frequency of the ''CT/TT'' genotypes was significantly increased in patients with hepatocellular carcinoma (HCC) versus controls (OR=1.438; P = 0.015) [R]. 

 

rs1713449

Parent Gene: TEP1

Importance: 2
Less common allele: T = 32%
More common allele: C = 68%
My Genotype: Log In