FSHB · rs11031005
Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied up to 2913 European ancestry individuals.
The effect Each copy of the C allele shifted the measure 0.232 lower; p = 2 × 10−8.
How common The C allele had a frequency of about 13% in the people studied.
Where it sits Chromosome 11, band 11p14.1 — in an intron of ARL14EP-DT.
What people read about alongside this
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
rs11031005 is a single position in the genome, in or near the FSHB gene. Published research associates it with sex hormone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Subjects that appear in the title or abstract of the same papers as this rsID include fertility (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
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.
GWAS Catalog, Eur J Hum Genet 2015, PMID:26014426. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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.
Sex hormone levels (rs11031005). MyGeneLog™. https://www.mygenelog.com/variants/rs11031005