We use cookies

Essential storage keeps the site working (sign-in, theme, this choice). We'd also like to load Google Analytics to understand, in aggregate, how the site is used — never your genetic data. See our Cookie Policy.

GSTM5 rs3768490: Understanding Your Genetic Skin Resilience

rs3768490
Skin & Photo-aging
Moderate evidenceGene: GSTM5

The rs3768490 variant is a single nucleotide polymorphism located within the GSTM5 gene. It is associated with cellular detoxification processes that may influence how skin cells manage oxidative stress and environmental damage.

What each genotype means

A/ALower attention

Typical detoxification capacity

This genotype represents the common variant for the GSTM5 gene in many populations. As GSTM5 is involved in cellular detoxification, this profile is generally considered to have standard enzyme function regarding oxidative stress management in the skin. Individual skin resilience remains influenced by a complex interplay of other genetic factors, sun exposure, and lifestyle habits.

This is a common genotype found across most global populations.

A/CLower attention

Typical detoxification capacity

Carrying one copy of the C allele alongside the A allele is common and generally associated with standard GSTM5 enzyme activity. While this gene plays a role in neutralizing oxidative stress, this specific genotype does not indicate a significant deviation from typical skin resilience. Maintaining a healthy lifestyle and protecting skin from environmental stressors remains the primary way to support skin health.

This heterozygous genotype is frequently observed in diverse populations worldwide.

C/CLower attention

Typical detoxification capacity

This genotype is a common variation of the GSTM5 gene. Research into this specific variant does not suggest a significant functional impairment or clinical difference in skin aging processes compared to other genotypes. Skin health is multifactorial, and this genotype should be viewed as part of the normal range of human genetic variation.

This genotype is common, with the C allele appearing at a global minor allele frequency of approximately 0.38.

What is rs3768490?

The rs3768490 variant is a specific genetic change, or single nucleotide polymorphism (SNP), located on chromosome 1. In the human genome, this variant sits within the GSTM5 gene, which stands for Glutathione S-Transferase Mu 5. A SNP represents a variation at a single position in the DNA sequence among individuals. For rs3768490, the variation involves the substitution of one nucleotide for another. Because this variant is located within a gene that plays a role in cellular defense, researchers study it to understand how subtle differences in our genetic code might influence biological pathways. It is cataloged in major genomic databases, including dbSNP, which tracks human genetic variation to help scientists map the functional landscape of the genome.

The Role of the GSTM5 Gene

The GSTM5 gene belongs to the glutathione S-transferase (GST) family, a group of enzymes that are critical for cellular detoxification. These enzymes help the body neutralize reactive molecules, including those generated by oxidative stress, environmental toxins, and carcinogens. By facilitating the conjugation of glutathione to various substrates, GST enzymes assist in making these potentially harmful substances more water-soluble and easier for the body to eliminate. Because skin is constantly exposed to external stressors like ultraviolet radiation and pollutants, the efficiency of these detoxification pathways is thought to be important for maintaining skin health. When these pathways are functioning optimally, they help protect cellular structures, such as collagen and elastin, from the damage that can lead to premature signs of aging.

Research and Evidence Strength

The association between GSTM5 variants and skin-related phenotypes is considered to be of moderate evidence strength. While the GST family is well-documented for its role in managing oxidative stress, specific links between the rs3768490 variant and clinical skin aging outcomes are still being explored. Current research often focuses on how genetic polymorphisms in antioxidant genes contribute to a predisposition for higher oxidative stress, which can accelerate skin deterioration. However, it is important to note that skin health is a complex, polygenic trait influenced by a combination of many genetic factors, lifestyle choices, and environmental exposures. Because of this complexity, the impact of a single SNP like rs3768490 is generally considered small, and findings can vary across different study populations and research designs.

Population Frequency

Genetic variants are distributed differently across global populations, and understanding these frequencies is a key part of genomic research. For rs3768490, the Global Minor Allele Frequency (GMAF) is approximately 0.3848. This indicates that the variant is relatively common in the general population. Because this frequency is high, it suggests that the variant is not a rare mutation but rather a common genetic polymorphism that has been maintained in the human gene pool. Researchers use these frequency data to ensure that genetic studies are representative and to help determine if a specific variant might have different implications depending on an individual's ancestral background. Large-scale projects like gnomAD provide these frequency estimates to help contextualize the prevalence of such variants.

Interpreting Your Genetic Information

Information about your genotype for rs3768490 provides a snapshot of one small piece of your genetic makeup. It is important to remember that this information is for educational purposes and does not constitute a medical diagnosis or a prediction of your skin's future health. Because skin aging is influenced by a wide array of factors—including diet, sun exposure, smoking, and thousands of other genetic variants—you cannot determine your skin's resilience based on this single SNP alone. If you are concerned about skin health, dermatological conditions, or the impact of specific medications on your health, you should consult with a qualified healthcare professional or a board-certified dermatologist. They can provide personalized advice based on your clinical history and physical examination, which are far more informative than any single genetic marker.

How common is this variant?

The rs3768490 variant is common, with a Global Minor Allele Frequency (GMAF) of approximately 0.3848 across diverse populations.

Frequently asked questions

Can I use this SNP to predict if I will get wrinkles?

No. Skin aging is a complex process influenced by many genes, environmental factors, and lifestyle habits. A single SNP like rs3768490 cannot predict specific skin outcomes.

What does the GSTM5 gene actually do?

The GSTM5 gene encodes an enzyme that helps the body neutralize toxins and manage oxidative stress. It is part of a larger family of enzymes involved in cellular detoxification.

Is this variant considered a 'bad' gene?

No. Genetic variants are simply differences in DNA sequences. Most common variants, including rs3768490, are part of normal human genetic diversity and are not inherently 'good' or 'bad'.

Should I change my skincare routine based on this result?

You should not change your medical or skincare routine based on a single genetic result. Always consult with a dermatologist for advice tailored to your specific skin type and health needs.

Sources & further reading

Educational information only, last refreshed 9/28/2026. Not medical advice — these associations describe population statistics, not individual predictions.

Curious what your genotype is for rs3768490?

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 — $29