Retinal thickness (functional principal component 5)
near SPRY2 · rs7996082
0 22Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others2Total2Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 43,152 European ancestry individuals; replicated in 1,179 Central or South Asian individuals, 1,161 African ancestry individuals.
The effect
Each copy of the T allele shifted the measure 14.5 higher (95% confidence interval 10.33-18.73); p = 1 × 10−11.
How common The T allele had a frequency of about 31% in the people studied.
Where it sits Chromosome 13, band 13q31.1 — between genes, 71.7 kb from SPRY2.
What each result means
C/CNo copy of the version the research linked to Retinal thickness (functional principal component 5). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Retinal thickness (functional principal component 5). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Retinal thickness (functional principal component 5). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2025 · PMID 39904976 · open access
Questions about rs7996082
What is rs7996082?
rs7996082 is a single position in the genome, in or near the near SPRY2 gene. Published research associates it with retinal thickness (functional principal component 5). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7996082 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs7996082 come from?
GWAS Catalog, Nature communications 2025, PMID:39904976. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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Quoting this page
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Retinal thickness (functional principal component 5) (rs7996082). MyGeneLog™. https://www.mygenelog.com/variants/rs7996082