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Basophil percentage in pregnancy

LINC02801 · rs4655950

What the study found

Who was studied 99,446 Chinese ancestry individuals; replicated in 46,518 Chinese ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.098 lower (95% confidence interval 0.084-0.112); p = 2 × 10−41.

How common The T allele had a frequency of about 36% in the people studied.

Where it sits Chromosome 1, band 1p22.3 — in an intron of LINC02801.

What each result means

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

Questions about rs4655950

What is rs4655950?

rs4655950 is a single position in the genome, in or near the LINC02801 gene. Published research associates it with basophil 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 rs4655950 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 rs4655950 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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Basophil percentage in pregnancy (rs4655950). MyGeneLog™. https://www.mygenelog.com/variants/rs4655950

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