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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 305,349 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.00216 mmol/L lower (95% confidence interval 0.0016-0.0027); p = 5 × 10−16.
How common The T allele had a frequency of about 25% in the people studied.
Where it sits Chromosome 11, band 11q23.3 — in an intron of NLRX1.
What each result means
C/CNo copy of the version the research linked to Calcium levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Calcium levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Calcium levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Circulation. Genomic and precision medicine · 2021 · PMID 33887147
Questions about rs561830
What is rs561830?
rs561830 is a single position in the genome, in or near the NLRX1 gene. Published research associates it with calcium levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs561830 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 rs561830 come from?
GWAS Catalog, Circulation. Genomic and precision medicine 2021, PMID:33887147. 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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