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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 2,466 Black/admixed ancestry individuals; replicated in up to 1,653 European, Hispanic, Asian or Black individuals.
The effect
Each copy of the A allele shifted the measure 1.53 higher (95% confidence interval 1.29-1.78); p = 7 × 10−34.
Where it sits Chromosome 22, band 22q11.23 — in an intron of UPB1.
What each result means
A/ATwo copies of the version the research linked to N-carbamoyl-beta-alanine levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to N-carbamoyl-beta-alanine levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to N-carbamoyl-beta-alanine levels. This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 35995766 · open access
Questions about rs145856948
What is rs145856948?
rs145856948 is a single position in the genome, in or near the UPB1 gene. Published research associates it with n-carbamoyl-beta-alanine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs145856948 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 rs145856948 come from?
GWAS Catalog, Nature communications 2022, PMID:35995766. 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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