Sensitive

Chronic kidney disease

MOB3C · rs139537100

Where this position leads

Conditions: Serum Metabolites in Chronic Kidney Disease, Kidney Function

rs139537100 Condition: Serum Metabolites in Chronic Kidney Disease Serum Metabolites in Chronic Kidney… Condition Condition: Kidney Function Kidney Function Condition rs139537100 rs139537100 MOB3C

What the study found

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

The effect The reported allele is C; the catalogue records no effect size ; p = 5 × 10−8.

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

Where it sits Chromosome 1, band 1p33 — in the 5′ untranslated region of MKNK1.

What each result means

C/C 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.
C/T One copy of the version the research linked to Chronic kidney disease. That is a smaller link than two copies.
T/T No copy of the version the research linked to Chronic kidney disease. This is the starting point the study compared everyone against.
Source

Questions about rs139537100

What is rs139537100?

rs139537100 is a single position in the genome, in or near the MOB3C 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 rs139537100 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 rs139537100 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 rs139537100 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 (rs139537100). MyGeneLog™. https://www.mygenelog.com/variants/rs139537100

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