[PMID 26515422] Discrete associations of the GCKR variant with metabolic risk in a Chinese population: longitudinal change analysis

rs780092

Parent Gene: GCKR

Importance: 3
Less common allele: G = 23%
More common allele: A = 77%
My Genotype: Log In
Risk Allele: G, G, A, A, A

Disease/Trait: Triglyceride Measurement

The G allele of rs780092 is reported to be associated with Triglyceride Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Triglycerides.

Disease/Trait: Serum Albumin Measurement

The G allele of rs780092 is reported to be associated with Serum Albumin Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Metabolite levels (ALB).

Disease/Trait: Triglyceride Measurement

The A allele of rs780092 is reported to be associated with Triglyceride Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Lipid traits (TG).

Disease/Trait: Total Cholesterol Measurement

The A allele of rs780092 is reported to be associated with Total Cholesterol Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Total cholesterol levels (BMI unadjusted).

Disease/Trait: Total Cholesterol Measurement

The A allele of rs780092 is reported to be associated with Total Cholesterol Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Total cholesterol levels (Asian initial, BMI unadjusted).