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Febrile seizures (MMR vaccine-related)

SCN1A · rs13004083

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Febrile seizures (MMR vaccine-related) compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Febrile seizures (MMR vaccine-related).
G/G Published research associates this genotype with typical/baseline likelihood of Febrile seizures (MMR vaccine-related) — no copies of the reported risk allele.
Source

Questions about rs13004083

What is rs13004083?

rs13004083 is a single position in the genome, in or near the SCN1A gene. Published research associates it with febrile seizures (mmr vaccine-related). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13004083 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 rs13004083 come from?

GWAS Catalog, Nat Genet 2014, PMID:25344690. 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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