Standard

Acquired hemolytic anemias (PheCode 283)

near COMMD8 · rs180692929

Where this position leads

Condition: Acquired Hemolytic Anemias

rs180692929 Condition: Acquired Hemolytic Anemias Acquired Hemolytic Anemias Condition rs180692929 rs180692929 near COMMD8

What the study found

Who was studied 273 African American or Afro-Caribbean cases, 121,331 African American or Afro-Caribbean controls, 687 European ancestry cases, 449,900 European ancestry controls.

The effect Each copy of the G allele shifted the measure 3.42 lower (95% confidence interval 3.4-3.44); p = 4 × 10−11.

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

Where it sits Chromosome 4, band 4p12 — between genes, 3.8 kb from COMMD8.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Acquired hemolytic anemias (PheCode 283) — no copies of the reported risk allele.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Acquired hemolytic anemias (PheCode 283).
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Acquired hemolytic anemias (PheCode 283) compared to the general population.
Source

Questions about rs180692929

What is rs180692929?

rs180692929 is a single position in the genome, in or near the near COMMD8 gene. Published research associates it with acquired hemolytic anemias (phecode 283). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs180692929 linked to?

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

Does having rs180692929 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 rs180692929 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

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Acquired hemolytic anemias (PheCode 283) (rs180692929). MyGeneLog™. https://www.mygenelog.com/variants/rs180692929

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