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Calcium-binding protein 39-like levels

CAB39L · rs35214871

What the study found

Who was studied 2,549 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.477 lower (95% confidence interval 0.4-0.55); p = 2 × 10−31.

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

Where it sits Chromosome 13, band 13q14.2 — in an intron of CAB39L.

What each result means

G/G No copy of the version the research linked to Calcium-binding protein 39-like levels. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to Calcium-binding protein 39-like levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Calcium-binding protein 39-like levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs35214871

What is rs35214871?

rs35214871 is a single position in the genome, in or near the CAB39L gene. Published research associates it with calcium-binding protein 39-like levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs35214871 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 rs35214871 come from?

GWAS Catalog, Nature genetics 2024, PMID:39528825. 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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Calcium-binding protein 39-like levels (rs35214871). MyGeneLog™. https://www.mygenelog.com/variants/rs35214871

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