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Degree of unsaturation (UKB data field 23443)

near PLA2G10GP · rs139110024

What the study found

Who was studied 88,268 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0831 lower (95% confidence interval 0.058-0.108); p = 8 × 10−11.

How common The T allele had a frequency of about 4% in the people studied.

Where it sits Chromosome 16, band 16p13.11 — between genes, 33.1 kb from PLA2G10GP.

What each result means

G/G No copy of the version the research linked to Degree of unsaturation (UKB data field 23443). This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Degree of unsaturation (UKB data field 23443). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Degree of unsaturation (UKB data field 23443). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs139110024

What is rs139110024?

rs139110024 is a single position in the genome, in or near the near PLA2G10GP gene. Published research associates it with degree of unsaturation (ukb data field 23443). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs139110024 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 rs139110024 come from?

GWAS Catalog, Biological psychiatry 2023, PMID:36764567. 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.

Degree of unsaturation (UKB data field 23443) (rs139110024). MyGeneLog™. https://www.mygenelog.com/variants/rs139110024

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