rs10190169 (CN5): trigeminal nerve disorder association
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Key takeaways
- This variant is linked to trigeminal nerve disorders.
- The association has a very low p-value 8e-12.
- It involves the CN5 gene region.
Key takeaways
- This variant is linked to trigeminal nerve disorders.
- The association has a very low p-value 8e-12.
- It involves the CN5 gene region.
What the research says This variant is associated with trigeminal nerve disorders. PMID 39024449 The effect size is 1.64 and the p-value is 8e-12 in about 627 thousand individuals. PMID 39024449
Reported associations
- Trigeminal nerve disorders: This variant is associated with trigeminal nerve disorders with a reported effect size of 1.64 and p-value 8e-12 in about 627 thousand individuals. PMID 39024449
Evidence quality The evidence comes from a genome-wide association study of 627 thousand individuals reporting a strong association with trigeminal nerve disorders (p=8e-12). The variant is the C allele at rs10190169 in the CN5 region. PMID 39024449
Last lifestyle considerations on file for this variant.
Frequently asked questions
What does rs10190169 mean?
It is a genetic variant in the CN5 gene that has been linked to trigeminal nerve disorders.
Is this SNP related to pain?
Yes it is associated with trigeminal nerve disorders which can cause facial pain.
Can I change my risk?
No the variant does not change disease risk on its own and no lifestyle changes are recommended.