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Reticulocyte count (UKB data field 30250)

near RN7SL554P · rs2326843

What the study found

Who was studied 394,642 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0175 lower (95% confidence interval 0.013-0.022); p = 1 × 10−12.

How common The A allele had a frequency of about 19% in the people studied.

Where it sits Chromosome 6, band 6p25.1 — between genes, 12.3 kb from RN7SL554P.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Reticulocyte count (UKB data field 30250) compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Reticulocyte count (UKB data field 30250).
G/G Published research associates this genotype with typical/baseline likelihood of Reticulocyte count (UKB data field 30250) — no copies of the reported risk allele.
Source

Questions about rs2326843

What is rs2326843?

rs2326843 is a single position in the genome, in or near the near RN7SL554P gene. Published research associates it with reticulocyte count (ukb data field 30250). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2326843 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 rs2326843 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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.

Reticulocyte count (UKB data field 30250) (rs2326843). MyGeneLog™. https://www.mygenelog.com/variants/rs2326843

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