The C allele of rs10889353 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 Cholesterol, total.
The C allele of rs10889353 is reported to be associated with Low Density Lipoprotein Cholesterol Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with LDL cholesterol.
The C allele of rs10889353 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.
The C allele of rs10889353 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.
rs10889353 is associated with Lipid Measurement (R) . It is reported to have a 0.033 unit decrease on Lipid metabolism phenotypes (TG.by.NMR, whole). No specific risk allele was identified in the study.
rs10889353 is associated with Lipid Measurement (R) . It is reported to have a 0.035 unit decrease on Lipid metabolism phenotypes (TG.by.NMR, fasting). No specific risk allele was identified in the study.
rs10889353 is associated with Lipid Measurement (R) . It is reported to have a 1.32 unit decrease on Lipid metabolism phenotypes (VLDL.medium, fasting). No specific risk allele was identified in the study.
rs10889353 is associated with Lipid Measurement (R) . It is reported to have a 1.3230000000000002 unit decrease on Lipid metabolism phenotypes (VLDL.small, whole). No specific risk allele was identified in the study.
rs10889353 is associated with Lipid Measurement (R) . It is reported to have a 2.688 unit decrease on Lipid metabolism phenotypes (VLDL.total, fasting). No specific risk allele was identified in the study.
rs10889353 is associated with Lipid Measurement (R) . It is reported to have a 2.9730000000000003 unit decrease on Lipid metabolism phenotypes (VLDL.total, whole). No specific risk allele was identified in the study.