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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 497 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.409 lower (95% confidence interval 0.29-0.53); p = 2 × 10−11.
Where it sits Chromosome 1, band 1q23.3 — in an intron of FCGR2C.
What each result means
C/CNo copy of the version the research linked to FCGR2B protein levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to FCGR2B protein levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to FCGR2B protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Scientific reports · 2024 · PMID 38565889 · open access
Questions about rs71519209
What is rs71519209?
rs71519209 is a single position in the genome, in or near the FCGR2C gene. Published research associates it with fcgr2b protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs71519209 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 rs71519209 come from?
GWAS Catalog, Scientific reports 2024, PMID:38565889. 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
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.
FCGR2B protein levels (rs71519209). MyGeneLog™. https://www.mygenelog.com/variants/rs71519209