Overview
rs2571598 is a genetic variant.
This variant is located on chromosome 7. The variations at position 100892018 are the genetic letters C/C, T/T, C/T
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 rs2571598 there are 3 currently known genotypes : C/C, T/T or C/T
Short Overview
Variant Location
rs2571598 is located on gene in chromsome 7. Use the genome browser to explore the location of rs2571598 and its genetic neighbourhood.
Conditions & Traits
rs2571598 affects the following conditions and traits:
There are currently 0 conditions and 0 traits associated with rs2571598.
Pathogenicity
rs2571598 affects the following conditions:
There are currently 0 conditions associated with rs2571598.
Genome Browser
This interactive browser visualizes what no human can see with the naked eye - our DNA. From a down to a specific position on a . The position you are looking at here is the exact location of variant rs. Explore more variants and their effects on the body by browsing left and right along the DNA strand.
Did you know genetic variants affect drugs?
Mutations are changes in genes and genetic variations are differences in the DNA among people. Variants are tiny changes in just one piece of the DNA while haplotypes are groups of these changes that usually come together.
Conditions & Traits of rs2571598
Current research shows 0 conditions and 0 traits.
Conditions
0Pharmacogenetics
The genetic variant rs2571598 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 rs2571598. 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.
Genotype
Level of evidence
Impacts
Summary
Breakdown
Drug Effect
Side Effects
Dosage
Individuals with the genotype C/C have decreased Drug Effect to RIVASTIGMINE.
more info
Breakdown
Drug Effect
Side Effects
Dosage
Individuals with the genotype C/T have decreased Drug Effect to RIVASTIGMINE.
more info
Breakdown
Drug Effect
Side Effects
Dosage
Individuals with the genotype T/T have increased Drug Effect to RIVASTIGMINE.
more info
Legend:
Increased
Decreased
No known effect
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
Individuals with the genotype C/C have decreased Drug Effect to RIVASTIGMINE.
Level of evidence
More info
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
Individuals with the genotype C/T have decreased Drug Effect to RIVASTIGMINE.
Level of evidence
More info
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
Individuals with the genotype T/T have increased Drug Effect to RIVASTIGMINE.
Level of evidence
More info
Legend:
Increased
Decreased
No known effect
Drugs related to rs2571598
All drugs that are linked to rs2571598 are listed here.
Studies and Sources
All of the resources below examine variant rs2571598
Xiaoyan Liu, Chunxian Yue, Zhi Xu, Hao Shu, Mengjia Pu, Hui Yu, Yongmei Shi, Liying Zhuang, Xiaohui Xu, Zhijun Zhang
Marcella Reale, Erica Costantini, Marta Di Nicola, Chiara D’Angelo, Sara Franchi, Marco D’Aurora, Maria Di Bari, Viviana Orlando, Sabrina Galizia, Serena Ruggieri, Liborio Stuppia, Claudio Gasperini, Ada Maria Tata, Valentina Gatta
Valentina Gatta, Guadalupe Mengod, Marcella Reale, Ada Maria Tata