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Who was studied 4,502 Danish ancestry cases, 51,049 Danish ancestry controls; replicated in 3,133 European ancestry cases, 32,917 European ancestry controls.
The effect
The reported allele is C; the catalogue records no effect size
; p = 2 × 10−13.
Where it sits Chromosome 3, band 3p14.3 — in an intron of ERC2.
What each result means
C/CTwo copies of the version the research linked to Febrile seizures. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Febrile seizures. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Febrile seizures. This is the starting point the study compared everyone against.
Brain : a journal of neurology · 2022 · PMID 35022648 · open access
Questions about rs4974130
What is rs4974130?
rs4974130 is a single position in the genome, in or near the ERC2 gene. Published research associates it with febrile seizures. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs4974130 linked to?
On MyGeneLog this position is linked to Febrile Seizures. The research behind each link, and its sources, are set out on that condition page.
Does having rs4974130 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 rs4974130 come from?
GWAS Catalog, Brain : a journal of neurology 2022, PMID:35022648. 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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