Sensitive

Chronic kidney disease

COL6A5 · rs200982668

Where this position leads

Conditions: Serum Metabolites in Chronic Kidney Disease, Kidney Function

rs200982668 Condition: Serum Metabolites in Chronic Kidney Disease Serum Metabolites in Chronic Kidney… Condition Condition: Kidney Function Kidney Function Condition rs200982668 rs200982668 COL6A5

What the study found

Who was studied 1,051 Japanese ancestry cases, 1,505 Japanese ancestry controls.

The effect The reported allele is G; the catalogue records no effect size ; p = 5 × 10−9.

How common The G allele had a frequency of about 99% in the people studied.

Where it sits Chromosome 3, band 3q22.1 — a missense change in COL6A5.

What each result means

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

Questions about rs200982668

What is rs200982668?

rs200982668 is a single position in the genome, in or near the COL6A5 gene. Published research associates it with chronic kidney 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 rs200982668 linked to?

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

Does having rs200982668 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 rs200982668 come from?

GWAS Catalog, International journal of molecular medicine 2018, PMID:30226566. 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.

Chronic kidney disease (rs200982668). MyGeneLog™. https://www.mygenelog.com/variants/rs200982668

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