Standard

mean platelet volume (MPV, mean, inv-norm transformed)

STARD10 · rs72964900

What the study found

Who was studied 335,593 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0616 higher (95% confidence interval 0.052-0.072); p = 3 × 10−33.

How common The C allele had a frequency of about 89% in the people studied.

Where it sits Chromosome 11, band 11q13.4 — in an intron of STARD10.

What each result means

C/C Two copies of the version the research linked to mean platelet volume (MPV, mean, inv-norm transformed). 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 mean platelet volume (MPV, mean, inv-norm transformed). That is a smaller link than two copies.
T/T No copy of the version the research linked to mean platelet volume (MPV, mean, inv-norm transformed). This is the starting point the study compared everyone against.
Source

Questions about rs72964900

What is rs72964900?

rs72964900 is a single position in the genome, in or near the STARD10 gene. Published research associates it with mean platelet volume (mpv, mean, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs72964900 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 rs72964900 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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mean platelet volume (MPV, mean, inv-norm transformed) (rs72964900). MyGeneLog™. https://www.mygenelog.com/variants/rs72964900

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