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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 14,076 East Asian ancestry individuals.
The effect
The reported allele is T; the catalogue records no effect size
; p = 4 × 10−14.
How common The T allele had a frequency of about 33% in the people studied.
Where it sits Chromosome 12, band 12q24.13 — between genes, 5 kb from NAA25.
What each result means
C/CNo copy of the version the research linked to Low-carbohydrate diet (LCD) score. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Low-carbohydrate diet (LCD) score. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Low-carbohydrate diet (LCD) score. That is the strongest link of the three results. A link in a study is not a diagnosis.
European journal of clinical nutrition · 2022 · PMID 35132194
Questions about rs147992802
What is rs147992802?
rs147992802 is a single position in the genome, in or near the near NAA25 gene. Published research associates it with low-carbohydrate diet (lcd) score. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs147992802 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 rs147992802 come from?
GWAS Catalog, European journal of clinical nutrition 2022, PMID:35132194. 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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