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Platelet count

TNPO1-DT · rs2338793

Where this position leads

Condition: Blood Cell Counts

rs2338793 Condition: Blood Cell Counts Blood Cell Counts Condition rs2338793 rs2338793 TNPO1-DT

What the study found

Who was studied 350,474 European ancestry individuals, 148,623 East Asian ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0316 lower (95% confidence interval 0.027-0.037); p = 8 × 10−33.

Where it sits Chromosome 5, band 5q13.2 — in an intron of TNPO1-DT.

What each result means

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

Questions about rs2338793

What is rs2338793?

rs2338793 is a single position in the genome, in or near the TNPO1-DT gene. Published research associates it with platelet count. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs2338793 linked to?

On MyGeneLog this position is linked to Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.

Does having rs2338793 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 rs2338793 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. 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 count (rs2338793). MyGeneLog™. https://www.mygenelog.com/variants/rs2338793

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