The cardiogenetics panel is used to identify specific regions of your genetic profile associated with an increased risk for cardiovascular disease. By analyzing the DNA of these regions, we are able to identify variants associated with this risk.
Variants are alternate sequences that differ from the normal DNA sequence. Carrying a risk variant does not mean you will necessarily suffer from cardiovascular disease; it means your risk is increased compared to someone who carries no copies of the risk variant. The results of this test can be used by healthcare professionals to create a treatment plan to complement your genetic risk factors.
The panel tests genetic variants in 5 regions:
Having the variant of 4q25 may increase your risk of atrial fibrillation, which causes an irregular heartbeat and risk of stroke¹.
Depending on which variants of region 9p21 you carry, you may have an increased risk of coronary artery disease²,³.
Those with the variant of KIF6 who are treated with statins have a lower risk of cardiovascular disease⁴.
Having the variant of APOE may increase your risk of Type III hyperlipoproteinemia, which prevents your body from correctly metabolizing fats. This can lead to atherosclerosis (a buildup of fats in your blood vessels), potentially increasing your risk of coronary artery disease and blood clots⁵.
Your chances of having heart disease or a stroke depends, in part, on which haptoglobin variant you have. This is especially true for those with diabetes, for whom cardiovascular disease is a major cause of death. Those with the Hp2-2 genotype and diabetes have a 500% greater risk of heart attack or stroke than those with the Hp1-1 genotype.
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