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Lymphocyte absolute value in pregnancy

LINC01934 · rs56169464

What the study found

Who was studied 99,851 Chinese ancestry individuals; replicated in 46,962 Chinese ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0537 lower (95% confidence interval 0.037-0.07); p = 1 × 10−10.

How common The C allele had a frequency of about 21% in the people studied.

Where it sits Chromosome 2, band 2q31.3 — in an intron of LINC01934.

What each result means

A/A No copy of the version the research linked to Lymphocyte absolute value in pregnancy. This is the starting point the study compared everyone against.
A/C One copy of the version the research linked to Lymphocyte absolute value in pregnancy. That is a smaller link than two copies.
C/C Two copies of the version the research linked to Lymphocyte 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 rs56169464

What is rs56169464?

rs56169464 is a single position in the genome, in or near the LINC01934 gene. Published research associates it with lymphocyte 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 rs56169464 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 rs56169464 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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Lymphocyte absolute value in pregnancy (rs56169464). MyGeneLog™. https://www.mygenelog.com/variants/rs56169464

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