Sensitive

Kidney stone disease

near TFAP2B · rs2206271

Where this position leads

Condition: Urolithiasis

rs2206271 Condition: Urolithiasis Urolithiasis Condition rs2206271 rs2206271 near TFAP2B

What the study found

Who was studied 13,746 East Asian ancestry cases, 241,425 East Asian ancestry controls, 17,969 European ancestry cases, 702,230 European ancestry controls.

The effect Each copy of the A allele carried 1.09 times the odds of Kidney stone disease (95% confidence interval 1.07-1.11); p = 7 × 10−20.

How common The A allele had a frequency of about 33% in the people studied.

Where it sits Chromosome 6, band 6p12.3 — between genes, 0.4 kb from TFAP2B.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Kidney stone disease compared to the general population.
A/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Kidney stone disease.
T/T Published research associates this genotype with typical/baseline likelihood of Kidney stone disease — no copies of the reported risk allele.
Source

Questions about rs2206271

What is rs2206271?

rs2206271 is a single position in the genome, in or near the near TFAP2B gene. Published research associates it with kidney stone disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs2206271 linked to?

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

Does having rs2206271 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 rs2206271 come from?

GWAS Catalog, Nature communications 2025, PMID:40216741. 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.

Kidney stone disease (rs2206271). MyGeneLog™. https://www.mygenelog.com/variants/rs2206271

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