rs117927012 - LINGO2 linked to oligodendroglioma
Upload your raw genetic data once, we'll show you which variants you carry and what the research says.
Key takeaways
- This SNP is linked to a brain tumor called oligodendroglioma.
- The association was found in about 9 thousand people with a strong signal (p=1e-6).
- It is not known to affect common health traits.
Key takeaways
- This SNP is linked to a brain tumor called oligodendroglioma.
- The association was found in about 9 thousand people with a strong signal (p=1e-6).
- It is not known to affect common health traits.
What the research says This variant is associated with Oligodendroglioma, reported effect size 5.76, p=1e-6, in about 9 thousand individuals PMID 36810956.
Reported associations Oligodendroglioma (brain tumor) - the variant is linked to this condition with a reported effect size of 5.76, p=1e-6, based on about 9 thousand people [PMID 36810956].
Evidence quality The GWAS catalog entry reports an association in roughly 9 thousand individuals with a p-value of 1e-6 and no replication data provided. No conflicting findings are reported. Last lifestyle considerations on file for this variant.
Frequently asked questions
What does the rs117927012 variant do?
It is a genetic change in the LINGO2 gene that has been linked to oligodendroglioma based on a GWAS study with p=1e-6 and about 9 thousand participants.
Is this SNP related to common health conditions?
The evidence only shows an association with brain tumor; no link to other common traits is reported.
How strong is the genetic signal for rs117927012?
The study reports a p-value of 1e-6 in roughly 9 thousand people, indicating a very strong association.