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Monocyte percentage in pregnancy

near RPL31P34 · rs7783398

What the study found

Who was studied 99,391 Chinese ancestry individuals; replicated in 46,695 Chinese ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0546 higher (95% confidence interval 0.038-0.072); p = 4 × 10−10.

How common The A allele had a frequency of about 32% in the people studied.

Where it sits Chromosome 7, band 7p22.1 — between genes, 2.1 kb from RPL31P34.

What each result means

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

Questions about rs7783398

What is rs7783398?

rs7783398 is a single position in the genome, in or near the near RPL31P34 gene. Published research associates it with monocyte percentage in pregnancy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7783398 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 rs7783398 come from?

GWAS Catalog, Nature genetics 2026, PMID:42509370. 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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Monocyte percentage in pregnancy (rs7783398). MyGeneLog™. https://www.mygenelog.com/variants/rs7783398

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