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Cerebrospinal fluid protein VIT levels

VIT · rs11124542

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

Strength of the evidence

3 / 4

Its strongest genetic-study result is p = 10⁻⁹³, with 3 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10⁻⁵⁰. 2: ClinVar from one lab (1 star), or p ≤ 10⁻²⁰. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10⁻⁸). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 2,524 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.439 higher (95% confidence interval 0.4-0.48); p = 1 × 10⁻⁹³.

How common The C allele had a frequency of about 41% in the people studied.

Where it sits Chromosome 2, band 2p22.2 — in an intron of VIT.

What each result means

A/A No copy of the version the research linked to Cerebrospinal fluid protein VIT levels. This is the starting point the study compared everyone against.

A/C One copy of the version the research linked to Cerebrospinal fluid protein VIT levels. That is a smaller link than two copies.

C/C Two copies of the version the research linked to Cerebrospinal fluid protein VIT levels. That is the strongest link of the three results. A link in a study is not a diagnosis.

Source

Low overlap of plasma and CSF protein quantitative trait loci affects protein discovery for neurological disease

Western D, Yang C, Timsina J, Liu M, Wang C, Campbell MC, Kotzbauer P, Perlmutter JS, Schindler SE, Morris JC, Holtzman DM, Alvarez I

and 12 more — show all

Pastor P, Wyss-Coray T, Marquié M, Cano A, Sung YJ, de Rojas I, Ruiz A, Budde J, Fernandez MV, Tarawneh R, Ibanez L, Cruchaga C

Science translational medicine · 2026 · PMID 42054495

Questions about rs11124542

What is rs11124542?

rs11124542 is a single position in the genome, in or near the VIT gene. Published research associates it with cerebrospinal fluid protein vit levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11124542 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 rs11124542 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

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.

Cerebrospinal fluid protein VIT levels (rs11124542). MyGeneLog™. https://www.mygenelog.com/variants/rs11124542

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