Standard

Folate-deficiency anemia (PheCode 281.13)

near RNU6-1059P · rs181869483

Where this position leads

Condition: Folate-deficiency Anemia

rs181869483 Condition: Folate-deficiency Anemia Folate-deficiency Anemia Condition rs181869483 rs181869483 near RNU6-10…

What the study found

Who was studied 450 African American or Afro-Caribbean cases, 120,910 African American or Afro-Caribbean controls, 903 European ancestry cases, 449,159 European ancestry controls.

The effect Each copy of the C allele shifted the measure 1.88 lower (95% confidence interval 1.82-1.94); p = 2 × 10−12.

How common The C allele had a frequency of about 100% in the people studied.

Where it sits Chromosome 4, band 4q22.3 — between genes, 103.7 kb from RNU6-1059P.

What each result means

C/C Two copies of the version the research linked to Folate-deficiency anemia (PheCode 281.13). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/G One copy of the version the research linked to Folate-deficiency anemia (PheCode 281.13). That is a smaller link than two copies.
G/G No copy of the version the research linked to Folate-deficiency anemia (PheCode 281.13). This is the starting point the study compared everyone against.
Source

Questions about rs181869483

What is rs181869483?

rs181869483 is a single position in the genome, in or near the near RNU6-1059P gene. Published research associates it with folate-deficiency anemia (phecode 281.13). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs181869483 linked to?

On MyGeneLog this position is linked to Folate-deficiency Anemia. The research behind each link, and its sources, are set out on that condition page.

Does having rs181869483 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 rs181869483 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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.

Folate-deficiency anemia (PheCode 281.13) (rs181869483). MyGeneLog™. https://www.mygenelog.com/variants/rs181869483

← See all variants