Standard

Renal function-related traits (sCR)

UMOD · rs11864909

Where this position leads

Condition: Kidney Function

rs11864909 Condition: Kidney Function Kidney Function Condition Topic: Kidneys Kidneys Topic rs11864909 rs11864909 UMOD

Solid lines are connections this site curates. Dashed lines mean the two ends share a research paper — worth knowing, and not a claim that one explains the other.

What the study found

Who was studied 42,257 East Asian, South Asian, and South East Asian ancestry individuals; replicated in 19,662 East Asian ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0052 mg/dl higher (95% confidence interval 0.0036-0.0068); p = 1 × 10−10.

How common The C allele had a frequency of about 81% in the people studied.

Where it sits Chromosome 16, band 16p12.3 — in an intron of PDILT.

What each result means

C/C Two copies of the version the research linked to Renal function-related traits (sCR). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Renal function-related traits (sCR). That is a smaller link than two copies.
T/T No copy of the version the research linked to Renal function-related traits (sCR). This is the starting point the study compared everyone against.
Source

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs11864909

What is rs11864909?

rs11864909 is a single position in the genome, in or near the UMOD gene. Published research associates it with renal function-related traits (scr). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11864909 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.

What do people read about alongside rs11864909?

Subjects that appear in the title or abstract of the same papers as this rsID include kidneys (4 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs11864909 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 rs11864909 come from?

GWAS Catalog, Nat Genet 2012, PMID:22797727. 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.

Renal function-related traits (sCR) (rs11864909). MyGeneLog™. https://www.mygenelog.com/variants/rs11864909

← See all variants