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Leukocyte telomere length

BFAR · rs56241312

What the study found

Who was studied 327,790 British ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.058 lower (95% confidence interval 0.042-0.074); p = 3 × 10−12.

How common The A allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 16, band 16p13.12 — in an intron of BFAR.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Leukocyte telomere length compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Leukocyte telomere length.
G/G Published research associates this genotype with typical/baseline likelihood of Leukocyte telomere length — no copies of the reported risk allele.
Source

Questions about rs56241312

What is rs56241312?

rs56241312 is a single position in the genome, in or near the BFAR gene. Published research associates it with leukocyte telomere length. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs56241312 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 rs56241312 come from?

GWAS Catalog, GeroScience 2024, PMID:38837026. 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.

Leukocyte telomere length (rs56241312). MyGeneLog™. https://www.mygenelog.com/variants/rs56241312

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