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Fasting insulin adjusted for BMI

near PTEN · rs10887773

What the study found

Who was studied 48,395 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, Other ancestry, Native American ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.056 lower (95% confidence interval 0.038-0.074); p = 5 × 10−10.

How common The T allele had a frequency of about 17% in the people studied.

Where it sits Chromosome 10, band 10q23.31 — between genes, 34.3 kb from PTEN.

What each result means

G/G No copy of the version the research linked to Fasting insulin adjusted for BMI. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Fasting insulin adjusted for BMI. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Fasting insulin adjusted for BMI. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs10887773

What is rs10887773?

rs10887773 is a single position in the genome, in or near the near PTEN gene. Published research associates it with fasting insulin adjusted for bmi. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10887773 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 rs10887773 come from?

GWAS Catalog, Diabetologia 2022, PMID:34951656. 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.

Fasting insulin adjusted for BMI (rs10887773). MyGeneLog™. https://www.mygenelog.com/variants/rs10887773

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