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Platelet side scatter

TPM4 · rs8104011

What the study found

Who was studied 29,675 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.267 SD units higher (95% confidence interval 0.21-0.33); p = 7 × 10−18.

How common The A allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 19, band 19p13.12 — in an intron of TPM4.

What each result means

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

Questions about rs8104011

What is rs8104011?

rs8104011 is a single position in the genome, in or near the TPM4 gene. Published research associates it with platelet side scatter. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs8104011 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 rs8104011 come from?

GWAS Catalog, Nature communications 2023, PMID:37596262. 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 side scatter (rs8104011). MyGeneLog™. https://www.mygenelog.com/variants/rs8104011

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