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Platelet crit in pregnancy

near GMCL2 · rs2961667

What the study found

Who was studied 95,572 Chinese ancestry individuals; replicated in 46,285 Chinese ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0674 higher (95% confidence interval 0.051-0.084); p = 1 × 10−15.

How common The G allele had a frequency of about 49% in the people studied.

What each result means

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

Questions about rs2961667

What is rs2961667?

rs2961667 is a single position in the genome, in or near the near GMCL2 gene. Published research associates it with platelet crit 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 rs2961667 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 rs2961667 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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Platelet crit in pregnancy (rs2961667). MyGeneLog™. https://www.mygenelog.com/variants/rs2961667

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