Standard

Creatinine levels

LRP2 · rs2673171

Where this position leads

Condition: Kidney Function

rs2673171 Condition: Kidney Function Kidney Function Condition rs2673171 rs2673171 LRP2

What the study found

Who was studied 153,950 Korean ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0591 lower (95% confidence interval 0.052-0.066); p = 2 × 10−69.

How common The G allele had a frequency of about 20% in the people studied.

Where it sits Chromosome 2, band 2q31.1 — in an intron of LRP2.

What each result means

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

Questions about rs2673171

What is rs2673171?

rs2673171 is a single position in the genome, in or near the LRP2 gene. Published research associates it with creatinine 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 rs2673171 linked to?

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

Does having rs2673171 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 rs2673171 come from?

GWAS Catalog, Nature communications 2025, PMID:40436827. 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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Creatinine levels (rs2673171). MyGeneLog™. https://www.mygenelog.com/variants/rs2673171

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