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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 80,003 European ancestry individuals.
The effect
The reported allele is T; the catalogue records no effect size
; p = 4 × 10−11.
How common The T allele had a frequency of about 5% in the people studied.
Where it sits Chromosome 9, band 9p24.1 — between genes, 63.2 kb from RANBP6.
What each result means
C/CPublished research associates this genotype with typical/baseline likelihood of Glycine 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 Glycine levels.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Glycine levels compared to the general population.
Nature communications · 2019 · PMID 30837465 · open access
Questions about rs13299380
What is rs13299380?
rs13299380 is a single position in the genome, in or near the near RANBP6 gene. Published research associates it with glycine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs13299380 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 rs13299380 come from?
GWAS Catalog, Nature communications 2019, PMID:30837465. 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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