rs7659604: what the research says
This variant is associated with a marginally increased risk for type-2 diabetes.
What each genotype means
Baseline risk profile
This genotype is associated with a baseline risk for type 2 diabetes in the context of this specific genetic variant. Research indicates that individuals with this genotype do not carry the specific allele associated with the increased risk observed in some studies.
This is a common genotype found in many global populations.
Slightly increased risk
Individuals with this genotype have been observed in some studies to have a marginally increased statistical association with type 2 diabetes. This association is modest, and it is important to remember that diabetes risk is influenced by a complex combination of many genetic factors and lifestyle choices.
This heterozygous genotype is common and found across diverse ancestral groups.
Baseline risk profile
While the T allele has been identified in some research as a risk-associated marker, studies have shown varying results regarding the risk profile for those who are homozygous for this allele. This genotype is generally considered to have a risk profile similar to the baseline, and it should not be viewed as a diagnostic indicator.
This genotype is common and observed frequently in general population cohorts.
Common
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This variant is linked to a slightly increased susceptibility to type-2 diabetes.
This SNP is one of several variants associated with type-2 diabetes risk.
This variant contributes to the genetic risk profile for type-2 diabetes.
This SNP has been identified as having an association with type-2 diabetes risk.
This variant near the LCT gene determines whether you keep producing lactase into adulthood. The genotype associated with lactase persistence means you likely tolerate dairy well.
Hair-color variant near KIT ligand.