Sensitive

Type 2 diabetes

ZFAND3 · rs9470794

Where this position leads

Condition: Type 2 Diabetes

rs9470794 Condition: Type 2 Diabetes Type 2 Diabetes Condition rs9470794 rs9470794 ZFAND3

What the study found

Who was studied 5,999 East Asian ancestry cases, 9,001 East Asian ancestry controls, 794 Malay ancestry cases, 1,240 Malay ancestry controls, 159 Filipino ancestry cases, 1,624 Filipino ancestry controls; replicated in 18,127 East Asian ancestry cases, 17,746 East Asian ancestry controls.

The effect Each copy of the C allele carried 1.12 times the odds of Type 2 diabetes (95% confidence interval 1.08-1.16); p = 2 × 10−10.

How common The C allele had a frequency of about 27% in the people studied.

Where it sits Chromosome 6, band 6p21.2 — in an intron of ZFAND3.

What each result means

C/C 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.
C/T One copy of the version the research linked to Type 2 diabetes. That is a smaller link than two copies.
T/T No copy of the version the research linked to Type 2 diabetes. This is the starting point the study compared everyone against.
Source

Questions about rs9470794

What is rs9470794?

rs9470794 is a single position in the genome, in or near the ZFAND3 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 rs9470794 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 rs9470794 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 rs9470794 come from?

GWAS Catalog, Nature genetics 2011, PMID:22158537. 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 (rs9470794). MyGeneLog™. https://www.mygenelog.com/variants/rs9470794

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