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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 11,358 European ancestry cases, 1,106,871 European ancestry controls.
The effect
Each copy of the G allele shifted the measure 0.155 lower (95% confidence interval 0.13-0.18); p = 4 × 10−26.
Where it sits Chromosome 5, band 5p15.33 — between genes, 87.9 kb from LINC02063.
What each result means
A/ANo copy of the version the research linked to Raynaud's syndrome. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Raynaud's syndrome. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Raynaud's syndrome. That is the strongest link of the three results. A link in a study is not a diagnosis.
Cell genomics · 2024 · PMID 39142284 · open access
Questions about rs7706161
What is rs7706161?
rs7706161 is a single position in the genome, in or near the near LINC02063 gene. Published research associates it with raynaud's syndrome. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7706161 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 rs7706161 come from?
GWAS Catalog, Cell genomics 2024, PMID:39142284. 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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