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T-cell surface glycoprotein CD5 levels

B4GALT1 · rs10113903

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.107 higher (95% confidence interval 0.08-0.134); p = 4 × 10−15.

How common The C allele had a frequency of about 31% in the people studied.

Where it sits Chromosome 9, band 9p21.1 — in an intron of B4GALT1.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of T-cell surface glycoprotein CD5 levels compared to the general population.
C/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with T-cell surface glycoprotein CD5 levels.
G/G Published research associates this genotype with typical/baseline likelihood of T-cell surface glycoprotein CD5 levels — no copies of the reported risk allele.
Source

Questions about rs10113903

What is rs10113903?

rs10113903 is a single position in the genome, in or near the B4GALT1 gene. Published research associates it with t-cell surface glycoprotein cd5 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10113903 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 rs10113903 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. 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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T-cell surface glycoprotein CD5 levels (rs10113903). MyGeneLog™. https://www.mygenelog.com/variants/rs10113903

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