rs11699GA
Rs11699 is a genetic variant that has been identified in various studies. It is a single nucleotide polymorphism (SNP) that affects the gene encoding the mTOR pathway. The variant appears to be associated with an increased risk of certain diseases, including Parkinson's disease and other neurodegenerative disorders.
The 'GA' designation refers to the specific base change associated with the variant, where a 'G' base
Studies have shown that individuals carrying this variant are more likely to experience certain adverse health
It is worth noting that the relationship between Rs11699 and disease risk is still an area of
Overall, the Rs11699 variant is an interesting area of study that may have important implications for our