Standard

Weight (UKB data field 21002)

ARHGAP15 · rs35028264

Where this position leads

Condition: Celiac Disease

rs35028264 Condition: Celiac Disease Celiac Disease Condition rs35028264 rs35028264 ARHGAP15

What the study found

Who was studied 394,642 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0155 higher (95% confidence interval 0.011-0.02); p = 2 × 10−11.

How common The T allele had a frequency of about 14% in the people studied.

Where it sits Chromosome 2, band 2q22.2 — in an intron of ARHGAP15.

What each result means

G/G No copy of the version the research linked to Weight (UKB data field 21002). This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Weight (UKB data field 21002). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Weight (UKB data field 21002). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs35028264

What is rs35028264?

rs35028264 is a single position in the genome, in or near the ARHGAP15 gene. Published research associates it with weight (ukb data field 21002). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs35028264 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 rs35028264 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 rs35028264 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

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.

Weight (UKB data field 21002) (rs35028264). MyGeneLog™. https://www.mygenelog.com/variants/rs35028264

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