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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 7,070 European ancestry cases, 248,810 European ancestry controls.
The effect
The reported allele is A; the catalogue records no effect size
; p = 2 × 10−8.
Where it sits Chromosome 10, band 10p15.1 — between genes, 4.6 kb from ASB13.
What each result means
A/ATwo copies of the version the research linked to Ectopic pregnancy. 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 Ectopic pregnancy. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Ectopic pregnancy. This is the starting point the study compared everyone against.
Human reproduction (Oxford, England) · 2023 · PMID 37877466 · open access
Questions about rs11598956
What is rs11598956?
rs11598956 is a single position in the genome, in or near the near ASB13 gene. Published research associates it with ectopic pregnancy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11598956 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 rs11598956 come from?
GWAS Catalog, Human reproduction (Oxford, England) 2023, PMID:37877466. 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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