Epilepsy and lamotrigine-induced maculopapular eruptions
CRAMP1L · rs79007183
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Who was studied 34 Korean ancestry cases, 1,080 Korean ancestry healthy controls.
The effect
Each copy of the A allele carried 14.00 times the odds of Epilepsy and lamotrigine-induced maculopapular eruptions; p = 3 × 10−10.
How common The A allele had a frequency of about 1% in the people studied.
Where it sits Chromosome 16, band 16p13.3 — in an intron of CRAMP1.
What each result means
A/ATwo copies of the version the research linked to Epilepsy and lamotrigine-induced maculopapular eruptions. 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 Epilepsy and lamotrigine-induced maculopapular eruptions. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Epilepsy and lamotrigine-induced maculopapular eruptions. This is the starting point the study compared everyone against.
rs79007183 is a single position in the genome, in or near the CRAMP1L gene. Published research associates it with epilepsy and lamotrigine-induced maculopapular eruptions. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs79007183 linked to?
On MyGeneLog this position is linked to Epilepsy. The research behind each link, and its sources, are set out on that condition page.
Does having rs79007183 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 rs79007183 come from?
GWAS Catalog, Epilepsy research 2015, PMID:26220383. 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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Epilepsy and lamotrigine-induced maculopapular eruptions (rs79007183). MyGeneLog™. https://www.mygenelog.com/variants/rs79007183