Standard

Sum eosinophil basophil counts

P4HA2 · rs186675820

What the study found

Who was studied 171,771 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.212 higher (95% confidence interval 0.16-0.27); p = 5 × 10−15.

How common The C allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 5, band 5q31.1 — in an intron of P4HA2.

What each result means

C/C Two copies of the version the research linked to Sum eosinophil basophil counts. 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 Sum eosinophil basophil counts. That is a smaller link than two copies.
T/T No copy of the version the research linked to Sum eosinophil basophil counts. This is the starting point the study compared everyone against.
Source

Questions about rs186675820

What is rs186675820?

rs186675820 is a single position in the genome, in or near the P4HA2 gene. Published research associates it with sum eosinophil basophil counts. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs186675820 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 rs186675820 come from?

GWAS Catalog, Cell 2016, PMID:27863252. 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.

Sum eosinophil basophil counts (rs186675820). MyGeneLog™. https://www.mygenelog.com/variants/rs186675820

← See all variants