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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 408,112 British individuals.
The effect
Each copy of the A allele shifted the measure 0.0157 lower (95% confidence interval 0.011-0.02); p = 4 × 10−11.
How common The A allele had a frequency of about 33% in the people studied.
Where it sits Chromosome 7, band 7p12.2 — in the 5′ untranslated region of IKZF1.
What each result means
A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Mean platelet volume compared to the general population.
A/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Mean platelet volume.
T/TPublished research associates this genotype with typical/baseline likelihood of Mean platelet volume — no copies of the reported risk allele.
rs11765436 is a single position in the genome, in or near the IKZF1 gene. Published research associates it with mean platelet volume. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11765436 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 rs11765436 come from?
GWAS Catalog, Cell 2020, PMID:32888494. 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.
Mean platelet volume (rs11765436). MyGeneLog™. https://www.mygenelog.com/variants/rs11765436