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Mean corpuscular hemoglobin

RAB11FIP3 · rs377134808

Where this position leads

Condition: Blood Cell Counts

rs377134808 Condition: Blood Cell Counts Blood Cell Counts Condition rs377134808 rs377134808 RAB11FIP3

What the study found

Who was studied 38,000 South Asian ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.604 lower (95% confidence interval 0.54-0.67); p = 5 × 10−71.

Where it sits Chromosome 16, band 16p13.3 — in an intron of RAB11FIP3.

What each result means

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

Questions about rs377134808

What is rs377134808?

rs377134808 is a single position in the genome, in or near the RAB11FIP3 gene. Published research associates it with mean corpuscular hemoglobin. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs377134808 linked to?

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

Does having rs377134808 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 rs377134808 come from?

GWAS Catalog, Nature communications 2024, PMID:39414775. 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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Mean corpuscular hemoglobin (rs377134808). MyGeneLog™. https://www.mygenelog.com/variants/rs377134808

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