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Mean corpuscular haemoglobin (UKB data field 30050)

near MPST · rs148341477

Where this position leads

Condition: Celiac Disease

rs148341477 Condition: Celiac Disease Celiac Disease Condition rs148341477 rs148341477 near MPST

What the study found

Who was studied 394,642 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.135 higher (95% confidence interval 0.094-0.176); p = 2 × 10−11.

How common The T allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 22, band 22q12.3 — between genes, 7.3 kb from MPST.

What each result means

G/G No copy of the version the research linked to Mean corpuscular haemoglobin (UKB data field 30050). This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Mean corpuscular haemoglobin (UKB data field 30050). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Mean corpuscular haemoglobin (UKB data field 30050). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs148341477

What is rs148341477?

rs148341477 is a single position in the genome, in or near the near MPST gene. Published research associates it with mean corpuscular haemoglobin (ukb data field 30050). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs148341477 linked to?

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

Does having rs148341477 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 rs148341477 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. 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 haemoglobin (UKB data field 30050) (rs148341477). MyGeneLog™. https://www.mygenelog.com/variants/rs148341477

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