Who was studied 33,572 Icelandic ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.038 lower (95% confidence interval -); p = 5 × 10−11.
How common The A allele had a frequency of about 42% in the people studied.
Where it sits Chromosome 5, band 5p15.33 — in an intron of CLPTM1L.
What each result means
A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Prostate-specific antigen levels compared to the general population.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Prostate-specific antigen levels.
G/GPublished research associates this genotype with typical/baseline likelihood of Prostate-specific antigen levels — no copies of the reported risk allele.
Nature communications · 2018 · PMID 30410027 · open access
Questions about rs381949
What is rs381949?
rs381949 is a single position in the genome, in or near the CLPTM1L gene. Published research associates it with prostate-specific antigen levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs381949 linked to?
On MyGeneLog this position is linked to Prostate-Specific Antigen (PSA) Levels. The research behind each link, and its sources, are set out on that condition page.
Does having rs381949 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 rs381949 come from?
GWAS Catalog, Nat Commun 2018, PMID:30410027. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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