Standard

Interleukin-1 receptor-associated kinase 4 levels

PUS7L · rs60813848

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.205 higher (95% confidence interval 0.16-0.25); p = 4 × 10−17.

How common The T allele had a frequency of about 7% in the people studied.

Where it sits Chromosome 12, band 12q12 — in the 3′ untranslated region of PUS7L.

What each result means

C/C No copy of the version the research linked to Interleukin-1 receptor-associated kinase 4 levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Interleukin-1 receptor-associated kinase 4 levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Interleukin-1 receptor-associated kinase 4 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs60813848

What is rs60813848?

rs60813848 is a single position in the genome, in or near the PUS7L gene. Published research associates it with interleukin-1 receptor-associated kinase 4 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs60813848 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 rs60813848 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. 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.

Interleukin-1 receptor-associated kinase 4 levels (rs60813848). MyGeneLog™. https://www.mygenelog.com/variants/rs60813848

← See all variants