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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 Up to 25,539 European ancestry individuals, 10,168 Japanese ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0266 higher (95% confidence interval 0.019-0.034); p = 4 × 10−11.
How common The A allele had a frequency of about 74% in the people studied.
Where it sits Chromosome 6, band 6p21.32 — between genes, 4.4 kb from PPT2.
What each result means
A/ATwo copies of the version the research linked to Serum total protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Serum total protein levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Serum total protein levels. This is the starting point the study compared everyone against.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs204999
What is rs204999?
rs204999 is a single position in the genome, in or near the near PPT2 gene. Published research associates it with serum total protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What do people read about alongside rs204999?
Subjects that appear in the title or abstract of the same papers as this rsID include infection and immunity (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs204999 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 rs204999 come from?
GWAS Catalog, Am J Hum Genet 2012, PMID:23022100. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
2 5452426224225Reads by AI crawlersClaude5ChatGPT2Google · Gemini4Perplexity2Meta AI6Microsoft · Copilot2Amazon2Apple4China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others25Total54Counted 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.
Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Serum total protein levels (rs204999). MyGeneLog™. https://www.mygenelog.com/variants/rs204999