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Cerebrospinal fluid protein BCHE levels

LINC01322 · rs12107166

What the study found

Who was studied 2,524 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.359 lower (95% confidence interval 0.31-0.41); p = 1 × 10−38.

How common The G allele had a frequency of about 13% in the people studied.

Where it sits Chromosome 3, band 3q26.1 — in an intron of LINC01322.

What each result means

G/G Two copies of the version the research linked to Cerebrospinal fluid protein BCHE levels. 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 Cerebrospinal fluid protein BCHE levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to Cerebrospinal fluid protein BCHE levels. This is the starting point the study compared everyone against.
Source

Questions about rs12107166

What is rs12107166?

rs12107166 is a single position in the genome, in or near the LINC01322 gene. Published research associates it with cerebrospinal fluid protein bche levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs12107166 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 rs12107166 come from?

GWAS Catalog, Science translational medicine 2026, PMID:42054495. 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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Cerebrospinal fluid protein BCHE levels (rs12107166). MyGeneLog™. https://www.mygenelog.com/variants/rs12107166

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