Understanding rs1171032562: A Rare Genetic Variant
The genetic variant rs1171032562 is a rare change in the human genome that does not reside within a known gene. It is currently being studied by researchers to determine if it plays any role in genetic ocular conditions.
What each genotype means
Typical genetic profile
This is the most common genotype observed in the general population. There is no evidence to suggest this specific genetic sequence is associated with any ocular conditions or clinical symptoms.
Carried by the vast majority of individuals across all global populations.
Rare variant carrier
You carry one copy of this rare variant. Current scientific literature provides limited evidence regarding its clinical significance, and it is currently being investigated for potential roles in ocular health. This finding does not constitute a diagnosis, and you should consult with a healthcare professional if you have concerns about your vision.
This genotype is extremely rare, observed at an allele frequency of approximately 0.0000026 in large-scale population databases.
Rare homozygous variant
You carry two copies of this rare variant. Because this variant is extremely uncommon, there is very limited research available to determine if this specific genotype has any impact on your health or vision. This result should be interpreted with caution and discussed with a medical professional or genetic counselor.
This genotype is exceptionally rare and has not been observed in most major population cohorts.
What is rs1171032562?
The identifier rs1171032562 refers to a specific single nucleotide polymorphism (SNP) in the human genome. In genetics, a SNP represents a variation at a single position in a DNA sequence among individuals. This particular variant is classified as intergenic, meaning it is located in the vast stretches of DNA that lie between protein-coding genes. Because it does not sit within a gene, it does not directly alter the instructions for building a protein. Instead, researchers investigate such variants to see if they might influence how nearby genes are regulated or expressed. As a rare variant, it is found in only a tiny fraction of the population, making it a subject of interest for scientists mapping the full landscape of human genetic diversity.
Research and Evidence
Currently, the evidence linking rs1171032562 to any specific health outcome or ocular condition is limited. In the field of genomics, many rare variants are identified in large-scale population databases like gnomAD, but their functional significance remains unknown. When a variant is rare, it is statistically difficult to determine if it contributes to a disease or is simply a benign piece of natural genetic variation. Because this variant is intergenic and lacks strong associations in major databases like the GWAS Catalog, it is not currently used in clinical diagnostics. Ongoing research continues to aggregate data from diverse populations to better understand whether such variants have any biological impact or if they are neutral markers of ancestry.
What You Can Do With This Information
It is important to understand that identifying a rare variant like rs1171032562 in your genetic data does not constitute a medical diagnosis. Because the scientific community has not established a clear link between this variant and any health condition, it is generally considered a finding of uncertain significance. If you have received this information through a genetic testing report, it is best to view it as a data point that is currently not actionable. You cannot use this information to predict your risk for eye conditions or to guide medical decisions. If you have concerns about your vision or family history of ocular health issues, the most appropriate step is to consult with an ophthalmologist or a certified genetic counselor who can provide context based on your full clinical picture.
How common is this variant?
The variant rs1171032562 is extremely rare, with a reported global population frequency of approximately 0.000003725.
Frequently asked questions
Is rs1171032562 a cause of blindness?
There is no scientific evidence to suggest that rs1171032562 causes blindness. It is a rare variant with limited research, and its role in human health is currently unknown.
Should I be worried if I have this variant?
No, you should not be worried. Most rare variants identified in genetic testing are benign, and there is no established clinical association for this specific SNP.
Where can I find more information on this variant?
You can search for the rsID on public databases like the NCBI dbSNP website or the gnomAD browser. These resources provide the most up-to-date frequency data from global research studies.
Does this variant affect my eye health?
Current research has not linked this variant to any specific eye health outcomes. If you have concerns about your vision, please consult an eye care professional.
Sources & further reading
Educational information only, last refreshed 9/16/2026. Not medical advice — these associations describe population statistics, not individual predictions.
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This variant is an uncharacterized single nucleotide variation with no established clinical significance.
This variant is an uncharacterized single nucleotide variation with no established clinical significance.
This variant is an uncharacterized single nucleotide variation with no established clinical significance.
This variant is an uncharacterized single nucleotide variation with no established clinical significance.
This variant is an uncharacterized single nucleotide variation with no established clinical significance.
This variant is an uncharacterized single nucleotide variation with no established clinical significance.