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Mean spheric corpuscular volume variance

SGCZ · rs577303028

What the study found

Who was studied 397,436 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 3.59 higher (95% confidence interval 2.53-4.64); p = 3 × 10−11.

Where it sits Chromosome 8, band 8p22 — in an intron of SGCZ.

What each result means

C/C Two copies of the version the research linked to Mean spheric corpuscular volume variance. 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 spheric corpuscular volume variance. That is a smaller link than two copies.
T/T No copy of the version the research linked to Mean spheric corpuscular volume variance. This is the starting point the study compared everyone against.
Source

Questions about rs577303028

What is rs577303028?

rs577303028 is a single position in the genome, in or near the SGCZ gene. Published research associates it with mean spheric corpuscular volume variance. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs577303028 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 rs577303028 come from?

GWAS Catalog, Nature communications 2025, PMID:40335489. 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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Mean spheric corpuscular volume variance (rs577303028). MyGeneLog™. https://www.mygenelog.com/variants/rs577303028

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