Standard

Glycated hemoglobin levels

near FN3KRP · rs9909940

What the study found

Who was studied 146,806 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0322 higher (95% confidence interval 0.029-0.035); p = 1 × 10−116.

How common The T allele had a frequency of about 31% in the people studied.

Where it sits Chromosome 17, band 17q25.3 — between genes, 0.8 kb from FN3KRP.

What each result means

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

Questions about rs9909940

What is rs9909940?

rs9909940 is a single position in the genome, in or near the near FN3KRP gene. Published research associates it with glycated hemoglobin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs9909940 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 rs9909940 come from?

GWAS Catalog, Nature genetics 2021, PMID:34059833. 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.

Glycated hemoglobin levels (rs9909940). MyGeneLog™. https://www.mygenelog.com/variants/rs9909940

← See all variants