Standard

Beta-microseminoprotein levels

ANTXRLP1 · rs4926051

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.444 higher (95% confidence interval 0.35-0.54); p = 3 × 10−20.

How common The C allele had a frequency of about 98% in the people studied.

Where it sits Chromosome 10, band 10q11.22 — in an intron of ANTXRLP1.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Beta-microseminoprotein 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 Beta-microseminoprotein levels.
G/G Published research associates this genotype with typical/baseline likelihood of Beta-microseminoprotein levels — no copies of the reported risk allele.
Source

Questions about rs4926051

What is rs4926051?

rs4926051 is a single position in the genome, in or near the ANTXRLP1 gene. Published research associates it with beta-microseminoprotein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4926051 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 rs4926051 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

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.

Beta-microseminoprotein levels (rs4926051). MyGeneLog™. https://www.mygenelog.com/variants/rs4926051

← See all variants