Standard
Waist-hip ratio
COBLL1 · rs13389219
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 each result means
C/C
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Waist-hip ratio compared to the general population.
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Waist-hip ratio.
T/T
Published research associates this genotype with typical/baseline likelihood of Waist-hip ratio — no copies of the reported risk allele.
Source
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
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Esko T,
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and 310 more — show all
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Nature genetics · 2013 · PMID 23563607 · open access
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.
Questions about rs13389219
What is rs13389219?
rs13389219 is a single position in the genome, in or near the COBLL1 gene. Published research associates it with waist-hip ratio. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What do people read about alongside rs13389219?
Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (2 papers), cholesterol and blood fats (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs13389219 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 rs13389219 come from?
GWAS Catalog, Nat Genet 2013, PMID:23563607. 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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