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Platelet count during second trimester of pregnancy

LINC02694 · rs79647915

What the study found

Who was studied 72,816 Chinese ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.1 lower (95% confidence interval 0.074-0.126); p = 6 × 10−14.

How common The C allele had a frequency of about 25% in the people studied.

Where it sits Chromosome 15, band 15q14 — in an intron of LINC02694.

What each result means

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

Questions about rs79647915

What is rs79647915?

rs79647915 is a single position in the genome, in or near the LINC02694 gene. Published research associates it with platelet count during second 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 rs79647915 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 rs79647915 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 second trimester of pregnancy (rs79647915). MyGeneLog™. https://www.mygenelog.com/variants/rs79647915

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