Sensitive

Type 2 diabetes

CDC123 · rs11257600

Where this position leads

Condition: Type 2 Diabetes

rs11257600 Condition: Type 2 Diabetes Type 2 Diabetes Condition rs11257600 rs11257600 CDC123

What the study found

Who was studied 2,277 African American cases, 3,098 East Asian ancestry cases, 3,704 European ancestry cases, 6,215 Hispanic/Latino cases, 2,939 South Asian ancestry cases, 2,283 African American controls, 2,921 East Asian ancestry controls, 3,514 European ancestry controls, 5,939 Hispanic/Latino controls, 3,022 South Asian ancestry controls.

The effect The reported allele is T; the catalogue records no effect size ; p = 6 × 10−17.

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

Where it sits Chromosome 10, band 10p13 — in an intron of CDC123.

What each result means

G/G No copy of the version the research linked to Type 2 diabetes. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Type 2 diabetes. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Type 2 diabetes. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs11257600

What is rs11257600?

rs11257600 is a single position in the genome, in or near the CDC123 gene. Published research associates it with type 2 diabetes. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11257600 linked to?

On MyGeneLog this position is linked to Type 2 Diabetes. The research behind each link, and its sources, are set out on that condition page.

Does having rs11257600 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 rs11257600 come from?

GWAS Catalog, Nature 2019, PMID:31118516. 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.

Type 2 diabetes (rs11257600). MyGeneLog™. https://www.mygenelog.com/variants/rs11257600

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