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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 3,647 European ancestry children.
The effect
Each copy of the A allele shifted the measure 0.632 lower (95% confidence interval 0.41-0.85); p = 2 × 10−8.
Where it sits Chromosome 3, band 3q26.31 — between genes, 6.2 kb from ACTG1P23.
What each result means
A/ATwo copies of the version the research linked to Mitochondrial DNA copy number. 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 Mitochondrial DNA copy number. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Mitochondrial DNA copy number. This is the starting point the study compared everyone against.
Human genomics · 2019 · PMID 30704525 · open access
Questions about rs144874692
What is rs144874692?
rs144874692 is a single position in the genome, in or near the NAALADL2 gene. Published research associates it with mitochondrial dna copy number. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs144874692 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 rs144874692 come from?
GWAS Catalog, Human genomics 2019, PMID:30704525. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Mitochondrial DNA copy number (rs144874692). MyGeneLog™. https://www.mygenelog.com/variants/rs144874692