Sensitive

Type 2 diabetes

HNF1A-AS1 · rs73226260

Where this position leads

Condition: Type 2 Diabetes

rs73226260 Condition: Type 2 Diabetes Type 2 Diabetes Condition rs73226260 rs73226260 HNF1A-AS1

What the study found

Who was studied 51,256 African, African American, East Asian, South Asian, European, Middle Eastern, admixed American, other or other admixed ancestry cases, 370,487 African, African American, East Asian, South Asian, European, Middle Eastern, admixed American, other or other admixed ancestry controls; replicated in 73,088 African, African American, East Asian, South Asian, European, Middle Eastern, admixed American, other or other admixed ancestry cases, 79,827 African, African American, East Asian, South Asian, European, Middle Eastern, admixed American, other or other admixed ancestry controls.

The effect Each copy of the G allele shifted the measure 0.16 higher (95% confidence interval 0.12-0.2); p = 9 × 10−13.

How common The G allele had a frequency of about 97% in the people studied.

Where it sits Chromosome 12, band 12q24.31 — in an intron of HNF1A-AS1.

What each result means

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

Questions about rs73226260

What is rs73226260?

rs73226260 is a single position in the genome, in or near the HNF1A-AS1 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 rs73226260 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 rs73226260 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 rs73226260 come from?

GWAS Catalog, Nature genetics 2024, PMID:39379762. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Type 2 diabetes (rs73226260). MyGeneLog™. https://www.mygenelog.com/variants/rs73226260

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