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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 8,744 East Asian ancestry individuals; replicated in 19,041 East Asian ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.257 higher; p = 6 × 10−134.
How common The T allele had a frequency of about 60% in the people studied.
Where it sits Chromosome 9, band 9q34.11 — inside CRAT.
What each result means
C/CNo copy of the version the research linked to Neonatal methylmalonyl + 3-hydroxy-isovalerylcarnitine (C4DC + C5-OH) levels (maternal genotype effect). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Neonatal methylmalonyl + 3-hydroxy-isovalerylcarnitine (C4DC + C5-OH) levels (maternal genotype effect). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Neonatal methylmalonyl + 3-hydroxy-isovalerylcarnitine (C4DC + C5-OH) levels (maternal genotype effect). That is the strongest link of the three results. A link in a study is not a diagnosis.
Cell genomics · 2024 · PMID 39389019 · open access
Questions about rs10988200
What is rs10988200?
rs10988200 is a single position in the genome, in or near the CRAT gene. Published research associates it with neonatal methylmalonyl + 3-hydroxy-isovalerylcarnitine (c4dc + c5-oh) levels (maternal genotype effect). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10988200 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 rs10988200 come from?
GWAS Catalog, Cell genomics 2024, PMID:39389019. 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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