Overview
rs1884613 is a genetic variant.
This variant is located on chromosome 20. The variations at position 44351775 are the genetic letters C/C, G/G, C/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 rs1884613 there are 3 currently known genotypes : C/C, G/G or C/G
Short Overview
Variant Location
rs1884613 is located on gene in chromsome 20. Use the genome browser to explore the location of rs1884613 and its genetic neighbourhood.
Conditions & Traits
rs1884613 affects the following conditions and traits:
There are currently 0 conditions and 0 traits associated with rs1884613.
Pathogenicity
rs1884613 affects the following conditions:
There are currently 0 conditions associated with rs1884613.
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 rs1884613
Current research shows 0 conditions and 0 traits.
Conditions
0Pharmacogenetics
The genetic variant rs1884613 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 rs1884613. 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
No summary available.
more info
Breakdown
Drug Effect
Side Effects
Dosage
Individuals with the genotype C/G have decreased Drug Effect to EFAVIRENZ.
more info
Breakdown
Drug Effect
Side Effects
Dosage
No summary available.
more info
Legend:
Increased
Decreased
No known effect
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
Individuals with the genotype C/G have decreased Drug Effect to EFAVIRENZ.
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
Drugs related to rs1884613
All drugs that are linked to rs1884613 are listed here.
Studies and Sources
All of the resources below examine variant rs1884613
Inês Barroso, Jian’an Luan, Eleanor Wheeler, Pamela Whittaker, Jon Wasson, Eleftheria Zeggini, Michael N. Weedon, Sarah Hunt, Ranganath Venkatesh, Timothy M. Frayling, Marcos Delgado, Rosalind J. Neuman, Jinghua Zhao, Richard Sherva, Benjamin Glaser, Mark Walker, Graham Hitman, Mark I. McCarthy, Andrew T. Hattersley, M. Alan Permutt, Nicholas J. Wareham, Panagiotis Deloukas
Rosalind J. Neuman, Jon Wasson, Gil Atzmon, Julio Wainstein, Yair Yerushalmi, Joseph Cohen, Nir Barzilai, Ilana Blech, Benjamin Glaser, M. Alan Permutt
H. P. Kang, X. Yang, R. Chen, B. Zhang, E. Corona, E. E. Schadt, A. J. Butte