Overview
rs1105879 is a genetic variant.
This variant is located on chromosome 2. The variations at position 233693556 are the genetic letters A/A, C/C, A/C
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 rs1105879 there are 3 currently known genotypes : A/A, C/C or A/C
Short Overview
Variant Location
rs1105879 is located on gene in chromsome 2. Use the genome browser to explore the location of rs1105879 and its genetic neighbourhood.
Conditions & Traits
rs1105879 affects the following conditions and traits:
There are currently 0 conditions and 0 traits associated with rs1105879.
Pathogenicity
rs1105879 affects the following conditions:
There are currently 0 conditions associated with rs1105879.
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 rs1105879
Current research shows 0 conditions and 0 traits.
Conditions
0Pharmacogenetics
The genetic variant rs1105879 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 rs1105879. 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 A/A have increased Drug Effect to ASPIRIN.
more info
Breakdown
Drug Effect
Side Effects
Dosage
No summary available.
more info
Breakdown
Drug Effect
Side Effects
Dosage
No summary available.
more info
Legend:
Increased
Decreased
No known effect
Genotype
Level of evidence
Impacts
Summary
Breakdown
Drug Effect
Side Effects
Dosage
Individuals with the genotype A/A have decreased Dosage to VALPROIC ACID.
more info
Breakdown
Drug Effect
Side Effects
Dosage
Individuals with the genotype A/C have increased Dosage to VALPROIC ACID.
more info
Breakdown
Drug Effect
Side Effects
Dosage
Individuals with the genotype C/C have increased Dosage to VALPROIC ACID.
more info
Legend:
Increased
Decreased
No known effect
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
Individuals with the genotype A/A have increased Drug Effect to ASPIRIN.
Level of evidence
More info
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
No summary available.
Level of evidence
More info
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
No summary available.
Level of evidence
More info
Legend:
Increased
Decreased
No known effect
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
Individuals with the genotype A/A have decreased Dosage to VALPROIC ACID.
Level of evidence
More info
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
Individuals with the genotype A/C have increased Dosage to VALPROIC ACID.
Level of evidence
More info
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
Individuals with the genotype C/C have increased Dosage to VALPROIC ACID.
Level of evidence
More info
Legend:
Increased
Decreased
No known effect
Drugs related to rs1105879
All drugs that are linked to rs1105879 are listed here.
Studies and Sources
All of the resources below examine variant rs1105879
Michael H. Court, Zhaohui Zhu, Gina Masse, Su X. Duan, Laura P. James, Jerold S. Harmatz, David J. Greenblatt
Harsh Sheth, Emma Northwood, Cornelia M. Ulrich, Dominique Scherer, Faye Elliott, Jennifer H. Barrett, David Forman, C. Roland Wolf, Gillian Smith, Michael S. Jackson, Mauro Santibanez-Koref, Robert Haile, Graham Casey, Mark Jenkins, Aung Ko Win, John L. Hopper, Loic Le Marchand, Noralane M. Lindor, Stephen N. Thibodeau, John D. Potter, John Burn, D. Timothy Bishop
Tomoko Yoshihama, Koya Fukunaga, Akira Hirasawa, Hiroyuki Nomura, Tomoko Akahane, Fumio Kataoka, Wataru Yamagami, Daisuke Aoki, Taisei Mushiroda