Standard

FCAMR protein levels

SLC2A2 · rs61791106

Where this position leads

Condition: Celiac Disease

Drug: Metformin

rs61791106 Condition: Celiac Disease Celiac Disease Condition Drug: Metformin Metformin Drug rs61791106 rs61791106 SLC2A2

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0666 lower (95% confidence interval 0.05-0.083); p = 1 × 10−16.

How common The A allele had a frequency of about 12% in the people studied.

Where it sits Chromosome 3, band 3q26.2 — in an intron of SLC2A2.

What each result means

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

Questions about rs61791106

What is rs61791106?

rs61791106 is a single position in the genome, in or near the SLC2A2 gene. Published research associates it with fcamr protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs61791106 linked to?

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

Does rs61791106 affect how medicines work?

SLC2A2 carries pharmacogenomic findings for Metformin. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.

Does having rs61791106 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 rs61791106 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. 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.

FCAMR protein levels (rs61791106). MyGeneLog™. https://www.mygenelog.com/variants/rs61791106

← See all variants