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Eosinophil count

LINC02954 · rs76738175

Where this position leads

Condition: Blood Cell Counts

rs76738175 Condition: Blood Cell Counts Blood Cell Counts Condition rs76738175 rs76738175 LINC02954

What the study found

Who was studied 86,890 East Asian ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.063 SD units higher (95% confidence interval 0.043-0.083); p = 6 × 10−10.

How common The C allele had a frequency of about 86% in the people studied.

Where it sits Chromosome 11, band 11q12.2 — in a non-coding transcript of LINC02954.

What each result means

C/C Two copies of the version the research linked to Eosinophil count. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Eosinophil count. That is a smaller link than two copies.
T/T No copy of the version the research linked to Eosinophil count. This is the starting point the study compared everyone against.
Source

Questions about rs76738175

What is rs76738175?

rs76738175 is a single position in the genome, in or near the LINC02954 gene. Published research associates it with eosinophil count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs76738175 linked to?

On MyGeneLog this position is linked to Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.

Does having rs76738175 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 rs76738175 come from?

GWAS Catalog, Cell 2020, PMID:32888493. 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.

Eosinophil count (rs76738175). MyGeneLog™. https://www.mygenelog.com/variants/rs76738175

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