Understanding rs113340062: A Genetic Variant Overview
The genetic variant rs113340062 is a single-nucleotide polymorphism located in an intergenic region of the human genome. It has been identified in genome-wide association studies (GWAS) as a marker with potential links to various phenotypic traits.
What each genotype means
Typical genetic profile
This genotype represents the most common form of this variant observed in general population studies. Current research has not established a specific clinical or trait-based significance for this genetic sequence. As this is an intergenic variant, it does not directly alter protein-coding regions.
The exact frequency of this genotype is currently unknown due to limited representation in large-scale population databases.
Typical genetic profile
This genotype represents a heterozygous state for this variant. Current research has not established a specific clinical or trait-based significance for this genetic sequence. As this is an intergenic variant, it does not directly alter protein-coding regions.
The exact frequency of this genotype is currently unknown due to limited representation in large-scale population databases.
Typical genetic profile
This genotype represents the alternative homozygous state for this variant. Current research has not established a specific clinical or trait-based significance for this genetic sequence. As this is an intergenic variant, it does not directly alter protein-coding regions.
The exact frequency of this genotype is currently unknown due to limited representation in large-scale population databases.
What is rs113340062?
A single-nucleotide polymorphism, or SNP, is a variation at a single position in a DNA sequence among individuals. The variant rs113340062 is classified as an intergenic SNP, meaning it is located in the DNA sequence between genes rather than within a gene that codes for a protein. Because it does not sit inside a gene, it does not directly alter the structure of a protein product. Instead, researchers study such variants to determine if they influence the regulation of nearby genes or serve as markers for other functional genetic changes. In the context of genomics, rs113340062 is cataloged in major databases that track variations across the human population to help scientists understand the architecture of complex traits.
Research and Associations
The primary evidence for rs113340062 comes from genome-wide association studies (GWAS). These studies scan the genomes of large groups of people to find statistical correlations between specific genetic markers and observable traits or health conditions. While rs113340062 has been included in such studies, the evidence strength for its association with any specific clinical outcome is currently considered moderate. In genomics, a moderate association suggests that while a statistical signal exists, it may not be a primary driver of a condition or may only be relevant in specific contexts. It is important to note that a statistical association in a GWAS does not necessarily imply causation. Further functional research is often required to understand if and how a specific intergenic variant contributes to biological processes.
Population Frequency and Interpretation
The frequency of rs113340062 across different human populations is currently not well-defined in public databases. Genetic variants often show significant differences in frequency based on ancestral background, and for many variants, comprehensive data across diverse global populations remains a work in progress. Because the population frequency is unknown, it is difficult to determine how common this variant is in the general public. When interpreting information about such variants, it is essential to recognize that genetic data is probabilistic rather than deterministic. Most complex traits are influenced by a combination of many genetic factors, environmental exposures, and lifestyle choices. Consequently, the presence of a specific genotype at this location does not provide a definitive prediction about an individual's health or physical characteristics.
Navigating Genetic Information
For individuals interested in their own genetic data, it is important to approach findings like rs113340062 with a clear understanding of their limitations. This variant is a research-grade marker, and its presence does not constitute a medical diagnosis or a clinical risk assessment. If you have received information about this variant from a direct-to-consumer genetic test, it is best viewed as a piece of scientific data rather than actionable health advice. You cannot use this information to make decisions about medical treatments or lifestyle changes. If you have concerns about your health or family history, the most appropriate step is to consult with a qualified healthcare provider or a genetic counselor. They can help place genetic findings into the context of your overall health, medical history, and clinical needs.
How common is this variant?
The population frequency for rs113340062 is currently unknown, as comprehensive data across diverse ancestral groups has not been established.
Frequently asked questions
What does it mean if a variant is intergenic?
An intergenic variant is located in the space between genes. This means it is not part of the instructions for building a protein, though it may still play a role in how genes are turned on or off.
Is rs113340062 linked to a specific disease?
While rs113340062 has been identified in genome-wide association studies, the evidence for a link to any specific disease is moderate. It is not currently considered a diagnostic marker for any condition.
Can I use this information to change my diet or medication?
No. You should never use information about genetic variants like rs113340062 to make changes to your diet or medication. Always consult with your doctor or pharmacist before making any health-related decisions.
Why is the population frequency unknown?
Genetic databases are constantly being updated as more people are sequenced. For many variants, there is simply not enough data from diverse populations yet to calculate an accurate frequency.
Sources & further reading
Educational information only, last refreshed 10/8/2026. Not medical advice — these associations describe population statistics, not individual predictions.
Curious what your genotype is for rs113340062?
Upload a raw DNA file from 23andMe, AncestryDNA, MyHeritage, or FamilyTreeDNA and see this variant — plus thousands more — interpreted in your full report.
Get my report — $29Related variants
A lead SNP associated with increased ZSCAN23 expression in pancreatic tissue, linked to longevity in recent GWAS findings.
A mitochondrial DNA mutation in the ND2 gene associated with electron transport chain function and longevity across multiple populations.
A genetic variant linked to ocular disease susceptibility and metabolic health, highlighting multifactorial etiology.
A pleiotropic locus identified in large-scale GWAS linking ocular disease risk to metabolic health.
This variant is associated with both ocular disease onset and metabolic conditions, suggesting shared biological pathways.
This SNP is identified as a pleiotropic marker associated with the onset of various eye diseases and metabolic comorbidities.