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Febrile seizures

near CD34 · rs1318653

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Febrile seizures — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2014, PMID:25344690)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Febrile seizures. (GWAS Catalog, Nat Genet 2014, PMID:25344690)
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Febrile seizures compared to the general population. (GWAS Catalog, Nat Genet 2014, PMID:25344690)
Source

Questions about rs1318653

What is rs1318653?

rs1318653 is a single position in the genome, in or near the near CD34 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.

Does having rs1318653 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 rs1318653 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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