Sensitive

Type 2 diabetes

YWHAH · rs117001013

Where this position leads

Condition: Type 2 Diabetes

rs117001013 Condition: Type 2 Diabetes Type 2 Diabetes Condition rs117001013 rs117001013 YWHAH

What the study found

Who was studied 148,726 European ancestry cases, 965,732 European ancestry controls.

The effect Each copy of the C allele shifted the measure 0.0474 higher (95% confidence interval 0.031-0.064); p = 1 × 10−8.

How common The C allele had a frequency of about 92% in the people studied.

Where it sits Chromosome 22, band 22q12.3 — in an intron of YWHAH.

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 rs117001013

What is rs117001013?

rs117001013 is a single position in the genome, in or near the YWHAH 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 rs117001013 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 rs117001013 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 rs117001013 come from?

GWAS Catalog, Nature genetics 2020, PMID:32541925. 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 (rs117001013). MyGeneLog™. https://www.mygenelog.com/variants/rs117001013

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