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Ribonucleoside-diphosphate reductase subunit M2 B (analyte X8925.25) levels

RRM2B · rs11778107

What the study found

Who was studied 3,506 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.318 higher (95% confidence interval 0.23-0.4); p = 2 × 10−13.

How common The C allele had a frequency of about 7% in the people studied.

Where it sits Chromosome 8, band 8q22.3 — in an intron of RRM2B.

What each result means

C/C Two copies of the version the research linked to Ribonucleoside-diphosphate reductase subunit M2 B (analyte X8925.25) levels. 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 Ribonucleoside-diphosphate reductase subunit M2 B (analyte X8925.25) levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to Ribonucleoside-diphosphate reductase subunit M2 B (analyte X8925.25) levels. This is the starting point the study compared everyone against.
Source

Questions about rs11778107

What is rs11778107?

rs11778107 is a single position in the genome, in or near the RRM2B gene. Published research associates it with ribonucleoside-diphosphate reductase subunit m2 b (analyte x8925.25) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11778107 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 rs11778107 come from?

GWAS Catalog, Nature genetics 2024, PMID:39528825. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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Ribonucleoside-diphosphate reductase subunit M2 B (analyte X8925.25) levels (rs11778107). MyGeneLog™. https://www.mygenelog.com/variants/rs11778107

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