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Glycated haemoglobin HbA1c levels (UKB data field 30750)

near HLA-DRB5 · rs2009684

Where this position leads

Condition: Celiac Disease

rs2009684 Condition: Celiac Disease Celiac Disease Condition rs2009684 rs2009684 near HLA-DRB5

Strength of the evidence

3 / 4

Its strongest genetic-study result is p = 10−60, with 1 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 394,642 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0411 higher (95% confidence interval 0.036-0.046); p = 6 × 10−61.

How common The A allele had a frequency of about 18% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 3.5 kb from HLA-DRB5.

How common each version is

AG
Korean KRGDB
A 14.2% · G 85.8%
Korean Korea4K
A 14.6% · G 85.4%
Japanese ToMMo
A 10.7% · G 89.3%
World gnomAD
A 16.9% · G 83.1%
World 1000 Genomes
A 14.4% · G 85.6%

The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study.

What each result means

A/A Two copies of the version the research linked to Glycated haemoglobin HbA1c levels (UKB data field 30750). 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 Glycated haemoglobin HbA1c levels (UKB data field 30750). That is a smaller link than two copies.
G/G No copy of the version the research linked to Glycated haemoglobin HbA1c levels (UKB data field 30750). This is the starting point the study compared everyone against.
Source

Questions about rs2009684

What is rs2009684?

rs2009684 is a single position in the genome, in or near the near HLA-DRB5 gene. Published research associates it with glycated haemoglobin hba1c levels (ukb data field 30750). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs2009684 linked to?

On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs2009684 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 rs2009684 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

Glycated haemoglobin HbA1c levels (UKB data field 30750) (rs2009684). MyGeneLog™. https://www.mygenelog.com/variants/rs2009684

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