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Who was studied 13,377 East Asian ancestry cases, 194,993 East Asian ancestry controls.
The effect
Each copy of the A allele carried 1.12 times the odds of Systemic lupus erythematosus (95% confidence interval 1.09-1.15); p = 2 × 10−13.
How common The A allele had a frequency of about 38% in the people studied.
Where it sits Chromosome 2, band 2q21.3 — between genes, 1.8 kb from MANEALP1.
What each result means
A/ATwo copies of the version the research linked to Systemic lupus erythematosus. 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 Systemic lupus erythematosus. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Systemic lupus erythematosus. This is the starting point the study compared everyone against.
Annals of the rheumatic diseases · 2021 · PMID 33272962 · open access
Questions about rs218174
What is rs218174?
rs218174 is a single position in the genome, in or near the DARS gene. Published research associates it with systemic lupus erythematosus. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs218174 linked to?
On MyGeneLog this position is linked to Systemic Lupus Erythematosus. The research behind each link, and its sources, are set out on that condition page.
Does having rs218174 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 rs218174 come from?
GWAS Catalog, Ann Rheum Dis 2020, PMID:33272962. 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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