Sensitive

Type 2 diabetes

PCGF3 · rs1531583

Where this position leads

Condition: Type 2 Diabetes

rs1531583 Condition: Type 2 Diabetes Type 2 Diabetes Condition rs1531583 rs1531583 PCGF3

What the study found

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

The effect Each copy of the G allele shifted the measure 0.0994 lower (95% confidence interval 0.077-0.121); p = 7 × 10−19.

How common The G allele had a frequency of about 96% in the people studied.

Where it sits Chromosome 4, band 4p16.3 — in an intron of PCGF3.

What each result means

G/G 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.
G/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 rs1531583

What is rs1531583?

rs1531583 is a single position in the genome, in or near the PCGF3 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 rs1531583 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 rs1531583 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 rs1531583 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 (rs1531583). MyGeneLog™. https://www.mygenelog.com/variants/rs1531583

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