Mitochondrial DNA heteroplasmy (chrM:302:A:AC case-only heteroplasmy)
near SNX5 · rs1884708
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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 65,137 European ancestry individuals, 431 East Asian ancestry individuals, 1,527 Central Asian ancestry individuals, 186 Hispanic or Latin American individuals, 958 African American or Afro-Caribbean individuals, 261 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals.
The effect
Each copy of the C allele shifted the measure 0.0319 higher (95% confidence interval 0.022-0.042); p = 5 × 10−10.
How common The C allele had a frequency of about 34% in the people studied.
Where it sits Chromosome 20, band 20p11.23 — between genes, 0.8 kb from SNX5.
What each result means
C/CTwo copies of the version the research linked to Mitochondrial DNA heteroplasmy (chrM:302:A:AC case-only heteroplasmy). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Mitochondrial DNA heteroplasmy (chrM:302:A:AC case-only heteroplasmy). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Mitochondrial DNA heteroplasmy (chrM:302:A:AC case-only heteroplasmy). This is the starting point the study compared everyone against.
rs1884708 is a single position in the genome, in or near the near SNX5 gene. Published research associates it with mitochondrial dna heteroplasmy (chrm:302:a:ac case-only heteroplasmy). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1884708 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 rs1884708 come from?
GWAS Catalog, Nature 2023, PMID:37587338. 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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Mitochondrial DNA heteroplasmy (chrM:302:A:AC case-only heteroplasmy) (rs1884708). MyGeneLog™. https://www.mygenelog.com/variants/rs1884708