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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 2,935 Qatari ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.413 higher (95% confidence interval 0.29-0.53); p = 4 × 10−11.
How common The T allele had a frequency of about 5% in the people studied.
Where it sits Chromosome 22, band 22q11.21 — in an intron of LINC00896.
What each result means
C/CPublished research associates this genotype with typical/baseline likelihood of Reticulon-4 receptor levels — no copies of the reported risk allele.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Reticulon-4 receptor levels.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Reticulon-4 receptor levels compared to the general population.
Human molecular genetics · 2023 · PMID 36168886 · open access
Questions about rs137981952
What is rs137981952?
rs137981952 is a single position in the genome, in or near the LINC00896 gene. Published research associates it with reticulon-4 receptor levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs137981952 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 rs137981952 come from?
GWAS Catalog, Human molecular genetics 2023, PMID:36168886. 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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