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T1 FreeSurfer aseg CC Posterior

FAM53B · rs4962692

What the study found

Who was studied 7,058 Chinese Han ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.115 lower (95% confidence interval 0.083-0.147); p = 1 × 10−12.

Where it sits Chromosome 10, band 10q26.13 — in an intron of FAM53B.

What each result means

A/A Two copies of the version the research linked to T1 FreeSurfer aseg CC Posterior. 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 T1 FreeSurfer aseg CC Posterior. That is a smaller link than two copies.
G/G No copy of the version the research linked to T1 FreeSurfer aseg CC Posterior. This is the starting point the study compared everyone against.
Source

Questions about rs4962692

What is rs4962692?

rs4962692 is a single position in the genome, in or near the FAM53B gene. Published research associates it with t1 freesurfer aseg cc posterior. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4962692 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 rs4962692 come from?

GWAS Catalog, Nature genetics 2024, PMID:38811844. 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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T1 FreeSurfer aseg CC Posterior (rs4962692). MyGeneLog™. https://www.mygenelog.com/variants/rs4962692

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