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Platelet count during third trimester of pregnancy

near LINC03002 · rs4896095

What the study found

Who was studied 72,816 Chinese ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0571 higher (95% confidence interval 0.044-0.07); p = 8 × 10−17.

How common The G allele had a frequency of about 31% in the people studied.

Where it sits Chromosome 6, band 6q23.3 — between genes, 61.9 kb from LINC03002.

What each result means

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

Questions about rs4896095

What is rs4896095?

rs4896095 is a single position in the genome, in or near the near LINC03002 gene. Published research associates it with platelet count during third trimester of pregnancy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4896095 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 rs4896095 come from?

GWAS Catalog, Blood 2024, PMID:38064665. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Platelet count during third trimester of pregnancy (rs4896095). MyGeneLog™. https://www.mygenelog.com/variants/rs4896095

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