rs17145750 appeared to be associated with the susceptibility to coronary artery disease (CAD), with the ''C'' alllele being significantly higher in the CAD group (P<0.01, OR=2.364) [R]. 

 

rs17145750

Parent Gene: MLXIPL

Importance: 4
Less common allele: T = 10%
More common allele: C = 90%
My Genotype: Log In
Risk Allele: C, T

Disease/Trait: Serum Gamma-Glutamyl Transferase Measurement

The C allele of rs17145750 is reported to be associated with Serum Gamma-glutamyl Transferase Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Liver enzyme levels (gamma-glutamyl transferase).

Disease/Trait: Lipoprotein Measurement

The T allele of rs17145750 is reported to be associated with Lipoprotein Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Metabolite levels (lipoprotein measures) (VLDL diameter).

Disease/Trait: Blood Metabolite Measurement

The T allele of rs17145750 is reported to be associated with Blood Metabolite Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Metabolite levels (lipoprotein measures) (VLDL diameter).