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Cerebrospinal fluid protein LAMB2 levels

LAMB2 · rs34759087

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.

What the study found

Who was studied 2,524 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.672 higher (95% confidence interval 0.63-0.71); p = 1 × 10⁻¹⁸⁹.

How common The T allele had a frequency of about 12% in the people studied.

Where it sits Chromosome 3, band 3p21.31 — a missense change in LAMB2.

What ClinVar records

Classification Benign for LAMB2-related infantile-onset nephrotic syndrome, Pierson syndrome; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 7 submitters), last evaluated 2026-02-02. ClinVar record 258606 NM_002292.4(LAMB2):c.2959G>A (p.Glu987Lys)

What this is ClinVar's aggregate record for this position (as of its 2026-10-12 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

C/C No copy of the version the research linked to Cerebrospinal fluid protein LAMB2 levels. This is the starting point the study compared everyone against.

C/T One copy of the version the research linked to Cerebrospinal fluid protein LAMB2 levels. That is a smaller link than two copies.

T/T Two copies of the version the research linked to Cerebrospinal fluid protein LAMB2 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 rs34759087

What is rs34759087?

rs34759087 is a single position in the genome, in or near the LAMB2 gene. Published research associates it with cerebrospinal fluid protein lamb2 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs34759087 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 rs34759087 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 LAMB2 levels (rs34759087). MyGeneLog™. https://www.mygenelog.com/variants/rs34759087

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