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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 9,260 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.06 lower (95% confidence interval 0.040-0.080); p = 3 × 10−12.
How common The A allele had a frequency of about 37% in the people studied.
Where it sits Chromosome 17, band 17q22 — a synonymous change in SMG8.
What each result means
A/ATwo copies of the version the research linked to Circulating myeloperoxidase levels (plasma). 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 Circulating myeloperoxidase levels (plasma). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Circulating myeloperoxidase levels (plasma). 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 rs6503905
What is rs6503905?
rs6503905 is a single position in the genome, in or near the C17orf71 gene. Published research associates it with circulating myeloperoxidase levels (plasma). 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 rs6503905?
Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (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 rs6503905 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 rs6503905 come from?
GWAS Catalog, Hum Mol Genet 2013, PMID:23620142. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
4 433234123223Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity3Meta AI4Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others23Total43Counted 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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