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Lymphocyte count

near MITA1 · rs566581671

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 38,000 South Asian ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.174 higher (95% confidence interval 0.14-0.21); p = 2 × 10⁻²⁰.

Where it sits Chromosome 8, band 8q21.13 — between genes, 161.3 kb from MITA1.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Lymphocyte count — no copies of the reported risk allele.

A/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Lymphocyte count.

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Lymphocyte count compared to the general population.

Source

Genetic architecture of routinely acquired blood tests in a British South Asian cohort

Jacobs BM, Stow D, Hodgson S, Zöllner J, Samuel M, Kanoni S, Bidi S, Walter K, Langenberg C, Dobson R, Finer S, Morton C

and 5 more — show all

Siddiqui MK, Martin HC, Pietzner M, Mathur R, van Heel DA

Genes & Health Research Team

Nature communications · 2024 · PMID 39414775 · open access

Questions about rs566581671

What is rs566581671?

rs566581671 is a single position in the genome, in or near the near MITA1 gene. Published research associates it with lymphocyte count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs566581671 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 rs566581671 come from?

GWAS Catalog, Nature communications 2024, PMID:39414775. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Lymphocyte count (rs566581671). MyGeneLog™. https://www.mygenelog.com/variants/rs566581671

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