rs4713586: Understanding Your Genetic Variant and Skin Resilience
The rs4713586 variant is a single nucleotide polymorphism located in an intergenic region of the human genome. It is frequently investigated in scientific studies exploring genetic markers associated with skin aging and dermatological resilience.
What each genotype means
Typical genetic profile
This genotype represents the common variant at this location. Research into this specific marker is limited, and it is primarily recognized for its role in tagging specific HLA haplotypes rather than direct skin-aging effects.
This is the most common genotype observed in most global populations.
Typical genetic profile
Carrying one copy of the T allele is a common variation at this site. Current scientific literature does not establish a significant or direct impact of this specific genotype on skin resilience or photo-aging.
This heterozygous genotype is found at moderate frequencies across diverse ancestral groups.
Typical genetic profile
This genotype is a recognized variation at this locus, which is often studied in the context of HLA region mapping. There is no robust evidence linking this specific genotype to clinical skin-aging phenotypes or dermatological conditions.
This genotype is less common than the C-allele variants but is present in most populations at low to moderate frequencies.
What is rs4713586 and Where is it Located?
The rs4713586 variant is a single nucleotide polymorphism, or SNP, which represents a variation at a single position in the DNA sequence. This specific variant is classified as intergenic, meaning it is located in the non-coding DNA regions between genes rather than within a gene that codes for a protein. According to genomic databases, rs4713586 is situated on chromosome 6. Because it resides in an intergenic region, researchers often study it to determine if it plays a regulatory role, perhaps influencing the expression of nearby genes or affecting how the body maintains skin integrity over time. While it does not directly code for a protein, its position in the genome makes it a subject of interest for those mapping the complex genetic architecture of human physical traits.
Research Associations and Evidence Strength
Scientific interest in rs4713586 primarily stems from its inclusion in studies regarding skin and photo-aging. In the field of dermatological genetics, researchers look for correlations between specific SNPs and observable traits like skin elasticity, wrinkle formation, or resilience to environmental stressors like ultraviolet radiation. The evidence linking rs4713586 to these outcomes is currently considered moderate. This means that while some studies have identified statistical associations, these findings are often part of broader, polygenic investigations where many variants contribute small effects to a single trait. It is important to note that skin aging is a complex phenotype influenced by a combination of genetic factors, lifestyle choices, and environmental exposures. Consequently, a single SNP like rs4713586 rarely acts as a definitive predictor of an individual's skin health or aging trajectory.
Population Frequency and Distribution
Genetic variants are distributed differently across global populations, and understanding these frequencies is essential for interpreting genomic data. For rs4713586, the reported population frequency is approximately 0.08, or 8%. This frequency represents the minor allele prevalence observed in large-scale genomic datasets. Because this variant is relatively common, it is found across various ancestral groups, though the exact percentage can fluctuate depending on the specific population being studied. Genomic databases like gnomAD and other population-wide studies provide these estimates to help scientists understand the prevalence of specific alleles. When interpreting your own genetic data, it is helpful to remember that these frequencies are averages derived from large cohorts and do not necessarily reflect the specific genetic makeup of every individual within a given ethnic or geographic group.
What You Can and Cannot Do With This Information
Learning about your genotype for rs4713586 can be an educational way to engage with your personal genomic data, but it is important to maintain realistic expectations. You can use this information to better understand the types of genetic markers that researchers are currently investigating in the context of skin health. However, you cannot use this information to diagnose a medical condition, predict your future skin appearance, or determine your risk for dermatological diseases. Genetic associations are statistical in nature and do not equate to medical certainty. If you have specific concerns about your skin health, such as changes in moles, persistent dryness, or signs of premature aging, the most effective approach is to consult a board-certified dermatologist. They can provide a professional assessment based on your clinical history and physical examination, which are far more informative than any single genetic variant.
How common is this variant?
The rs4713586 variant has a reported minor allele frequency of approximately 0.08 across diverse populations.
Frequently asked questions
Is rs4713586 a cause of skin aging?
No, rs4713586 is not considered a direct cause of skin aging. It is a genetic marker associated with the trait in statistical studies, but skin aging is a complex process influenced by many genes and environmental factors.
Can I use this SNP to predict if I will get wrinkles?
No, you cannot use this SNP to predict your future skin appearance. Genetic markers like rs4713586 provide only a small piece of a much larger puzzle and cannot account for lifestyle factors like sun exposure, diet, and skincare habits.
Where can I find more information about my specific genotype?
You can look up your rsID in public databases like dbSNP or the GWAS Catalog. These resources provide the most current scientific literature and research findings regarding specific genetic variants.
Should I change my skincare routine based on this variant?
No, you should not change your skincare routine based on this variant. Always consult with a dermatologist for personalized advice on skin health and the best products for your specific skin type and needs.
Sources & further reading
Educational information only, last refreshed 10/2/2026. Not medical advice — these associations describe population statistics, not individual predictions.
Curious what your genotype is for rs4713586?
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
Variants in this gene are linked to protein activity levels that may impact dermal microvasculature and skin health.
This variant is associated with RNA editing processes that may influence cellular responses relevant to skin tissue integrity and aging.
This variant in the NPC1 gene is involved in lipid trafficking, which is critical for maintaining the skin barrier and preventing premature photo-aging.
Suggestive loci and novel marker identified for facial skin sebum/oil traits and photo-aging parameters in GWAS.
Variant associated with facial skin aging and sensitivity phenotypes in Asian population GWAS.
This variant in the glutathione S-transferase gene is involved in cellular detoxification processes that may influence skin resilience against oxidative stress.
