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Group 10 secretory phospholipase A2 levels

LINC02571 · rs115971093

What the study found

Who was studied 2,917 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.395 higher (95% confidence interval 0.3-0.49); p = 7 × 10−15.

How common The A allele had a frequency of about 8% in the people studied.

Where it sits Chromosome 6, band 6p21.33 — in an intron of LINC02571.

What each result means

A/A Two copies of the version the research linked to Group 10 secretory phospholipase A2 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Group 10 secretory phospholipase A2 levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Group 10 secretory phospholipase A2 levels. This is the starting point the study compared everyone against.
Source

Questions about rs115971093

What is rs115971093?

rs115971093 is a single position in the genome, in or near the LINC02571 gene. Published research associates it with group 10 secretory phospholipase a2 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs115971093 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 rs115971093 come from?

GWAS Catalog, Nature communications 2021, PMID:34857772. 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.

Group 10 secretory phospholipase A2 levels (rs115971093). MyGeneLog™. https://www.mygenelog.com/variants/rs115971093

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