A0A0J9YXF2 protein level (protein group normalized intensity)
near PON2 · rs17879277
0 112216Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others6Total11Counted 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 1,242 European, Hispanic or African ancestry individuals; replicated in 325 Arab, Indian or Filipino ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.933 lower (95% confidence interval 0.86-1); p = 2 × 10−152.
How common The C allele had a frequency of about 23% in the people studied.
Where it sits Chromosome 7, band 7q21.3 — between genes, 3.5 kb from PON2.
What each result means
A/ANo copy of the version the research linked to A0A0J9YXF2 protein level (protein group normalized intensity). This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to A0A0J9YXF2 protein level (protein group normalized intensity). That is a smaller link than two copies.
C/CTwo copies of the version the research linked to A0A0J9YXF2 protein level (protein group normalized intensity). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2025 · PMID 41310232 · open access
Questions about rs17879277
What is rs17879277?
rs17879277 is a single position in the genome, in or near the near PON2 gene. Published research associates it with a0a0j9yxf2 protein level (protein group normalized intensity). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs17879277 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 rs17879277 come from?
GWAS Catalog, Nature genetics 2025, PMID:41310232. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 112216Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others6Total11Counted 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.
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A0A0J9YXF2 protein level (protein group normalized intensity) (rs17879277). MyGeneLog™. https://www.mygenelog.com/variants/rs17879277