Intergenic rs138684226: What Your Genotype Means
The rs138684226 variant is an intergenic single nucleotide polymorphism that has been identified in research regarding facial skin phenotypes. It is currently being studied for its potential statistical association with skin hydration properties.
What each genotype means
Typical skin hydration profile
This genotype is associated with baseline skin hydration properties identified in facial phenotype research. Current evidence is limited, and individual skin health is influenced by many genetic and environmental factors.
Frequency varies by ancestry, but this is a common genotype in many populations.
Typical skin hydration profile
This genotype is associated with baseline skin hydration properties identified in facial phenotype research. Current evidence is limited, and individual skin health is influenced by many genetic and environmental factors.
Frequency varies by ancestry, but this is a common genotype in many populations.
Typical skin hydration profile
This genotype is associated with baseline skin hydration properties identified in facial phenotype research. Current evidence is limited, and individual skin health is influenced by many genetic and environmental factors.
Frequency varies by ancestry, but this is a common genotype in many populations.
What is the rs138684226 Variant?
The rs138684226 variant is a single nucleotide polymorphism (SNP) located in an intergenic region of the human genome. Intergenic regions are the stretches of DNA that lie between genes and do not code for proteins themselves. While these regions were once referred to as 'junk DNA,' modern genomics has revealed that they often contain regulatory elements that control when and how genes are turned on or off. By studying SNPs in these areas, researchers can identify regulatory switches that influence various physical traits. The rs138684226 variant is one such marker that has emerged from large-scale genomic studies looking at facial characteristics and skin health.
Associations with Skin Hydration
Recent facial phenotype genome-wide association studies (GWAS) have highlighted rs138684226 in the context of skin hydration. Skin hydration is a complex trait influenced by a combination of genetic factors, environmental exposures, and lifestyle choices. The skin barrier, which is essential for maintaining moisture, relies on various biological pathways, including those involving filaggrin and aquaporins. While the exact mechanism by which this intergenic variant influences skin moisture is not fully understood, its identification in GWAS suggests it may be linked to the regulatory networks that govern skin barrier function. The evidence for this association is considered moderate, as skin traits are highly polygenic and influenced by many different genetic markers across the entire genome.
Understanding the Limits of Genetic Data
It is important to approach findings regarding skin-related genetic variants with a clear understanding of their limitations. Genetic associations identified in research studies are statistical in nature and describe trends observed in large populations. They do not provide a definitive prediction of an individual's skin type or hydration levels. Many factors, such as diet, climate, skincare routines, and age, play a much larger role in skin health than any single genetic variant. Consequently, this information should not be used to make medical decisions or to diagnose skin conditions. If you have concerns about your skin health, such as chronic dryness or irritation, it is best to consult with a dermatologist who can provide professional guidance based on your specific needs.
The Future of Genetic Skin Research
Research into the genetic basis of cosmetic and dermatological phenotypes is still in its early stages. As scientists continue to map the human genome and conduct more diverse studies, our understanding of how specific variants like rs138684226 contribute to skin characteristics will likely improve. Currently, the field is moving toward identifying how these markers might eventually inform personalized skincare approaches. However, we are not yet at a point where a simple genetic test can dictate a perfect skincare regimen. For now, the most effective way to maintain skin health remains following evidence-based practices, such as using appropriate moisturizers, protecting the skin from UV damage, and maintaining a healthy lifestyle, rather than focusing on individual genetic markers.
How common is this variant?
The population frequency for this variant is not specifically documented in standard catalogs, and its prevalence may vary significantly across different ancestral groups.
Frequently asked questions
What does 'intergenic' mean?
Intergenic refers to the DNA sequences located between genes. These regions do not code for proteins but often contain important regulatory sequences that control gene activity.
Can this variant predict my skin type?
No, this variant cannot predict your skin type. Skin traits are complex and influenced by many genetic and environmental factors, making it impossible to determine skin type from a single SNP.
Is there a test for this skin variant?
While some direct-to-consumer genetic tests may include various SNPs, there is no clinical test for rs138684226. It is currently a subject of research rather than a diagnostic tool.
How can I improve my skin hydration?
You can improve skin hydration by using gentle cleansers, applying moisturizers regularly, staying hydrated, and protecting your skin from harsh environmental conditions. Consult a dermatologist for advice tailored to your skin.
Sources & further reading
Educational information only, last refreshed 11/4/2026. Not medical advice — these associations describe population statistics, not individual predictions.
Curious what your genotype is for rs138684226?
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 cross-ancestral 3' UTR variant identified at the 13q13 locus linked to head and neck cancer subsites.
The rare allele of this variant is associated with a reduced risk of breast cancer in BRCA2 mutation carriers.
This intronic variant shows significant interaction with sleep traits in relation to language cognitive domains.
This variant is associated with increased sleep duration in multi-ancestry genomic studies.
A rare deleterious mutation in the melanopsin gene that renders the protein non-functional and causes delayed sleep-wake phase disorder.
A driver SNP associated with Primary Antiphospholipid Syndrome (PAPS) that influences disease susceptibility.
