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Monocyte absolute value in pregnancy

near EEIG1 · rs56805858

What the study found

Who was studied 99,434 Chinese ancestry individuals; replicated in 46,685 Chinese ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0613 higher (95% confidence interval 0.043-0.079); p = 3 × 10−11.

How common The T allele had a frequency of about 17% in the people studied.

Where it sits Chromosome 9, band 9q34.11 — between genes, 22.9 kb from EEIG1.

What each result means

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

Questions about rs56805858

What is rs56805858?

rs56805858 is a single position in the genome, in or near the near EEIG1 gene. Published research associates it with monocyte absolute value 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 rs56805858 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 rs56805858 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 absolute value in pregnancy (rs56805858). MyGeneLog™. https://www.mygenelog.com/variants/rs56805858

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