Standard

Cerebrospinal fluid protein GPI levels

CD163L1 · rs76502535

What the study found

Who was studied 2,524 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.581 lower (95% confidence interval 0.48-0.68); p = 4 × 10−30.

How common The T allele had a frequency of about 3% in the people studied.

Where it sits Chromosome 12, band 12p13.31 — in an intron of CD163L1.

What each result means

C/C No copy of the version the research linked to Cerebrospinal fluid protein GPI 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 GPI levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Cerebrospinal fluid protein GPI levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs76502535

What is rs76502535?

rs76502535 is a single position in the genome, in or near the CD163L1 gene. Published research associates it with cerebrospinal fluid protein gpi levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs76502535 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 rs76502535 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 GPI levels (rs76502535). MyGeneLog™. https://www.mygenelog.com/variants/rs76502535

← See all variants