rs112563513

rs112563513 is a genetic variant on gene RYR1 associated with Central core disease and Malignant hyperthermia of anesthesia.

This variant is located on chromosome 19. The variations at position 38499223 are the genetic letters A/A, G/G, A/G

Since humans have each twice (one from each parent), these letter-variations occur on both chromosomes. People can have the same or different letters on both chromosomes. Every person's individual variation combination is referred to as genotype. For variant rs112563513 there are 3 currently known genotypes : A/A, G/G or A/G

The different genotypes of variant rs112563513 can affect the likelyhood of developing certain traits or conditions. Current research shows that 2 conditions and 0 traits are associated with rs112563513. The following table shows the relationship between genotypes and conditions and traits.

The genetic variant rs112563513 impacts how certain medications work in the body. This difference may cause some of us to require different dosage amounts to achieve the desired effects, while others might experience more apparent side-effects. As a result, healthcare providers may need to adjust prescriptions for those individuals with rs112563513. Ultimately, understanding our genetic makeup helps improve the overall effectiveness and usability of medications. Tailoring treatments based on genetics ensures a safer, more personalized healthcare experience.