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Hematocrit

near RAI14-DT · rs10066469

What the study found

Who was studied 737,823 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals.

The effect The reported allele is A; the catalogue records no effect size ; p = 1 × 10−21.

How common The A allele had a frequency of about 47% in the people studied.

Where it sits Chromosome 5, band 5p13.2 — between genes, 151.5 kb from RAI14-DT.

What each result means

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

Questions about rs10066469

What is rs10066469?

rs10066469 is a single position in the genome, in or near the near RAI14-DT gene. Published research associates it with hematocrit. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10066469 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 rs10066469 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.

Hematocrit (rs10066469). MyGeneLog™. https://www.mygenelog.com/variants/rs10066469

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