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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 313,387 European ancestry individuals, 5,576 African ancestry individuals, 6,696 South Asian ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0229 higher (95% confidence interval 0.017-0.029); p = 1 × 10−12.
Where it sits Chromosome 19, band 19q13.41 — between genes, 0.8 kb from SPACA6-AS1.
What each result means
A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Calcium levels compared to the general population.
A/CPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Calcium levels.
C/CPublished research associates this genotype with typical/baseline likelihood of Calcium levels — no copies of the reported risk allele.
Nature genetics · 2021 · PMID 33462484 · open access
Questions about rs1868940
What is rs1868940?
rs1868940 is a single position in the genome, in or near the near SPACA6-AS1 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 rs1868940 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 rs1868940 come from?
GWAS Catalog, Nature genetics 2021, PMID:33462484. 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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