Genetic variation
rs606231422
Overview
rs606231422 is a genetic variant on gene CTLA4.
This variant is located on chromosome 2. The variations at position 203870684 are the genetic letters
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 rs606231422 there are 0 currently known genotypes .
Short Overview
Variant Location
rs606231422 is located on gene CTLA4 in chromsome 2. Use the genome browser to explore the location of rs606231422 and its genetic neighbourhood.
Conditions & Traits
rs606231422 affects the following conditions and traits:
There are currently 0 conditions and 0 traits associated with rs606231422.
Pathogenicity
rs606231422 affects the following conditions:
There are currently 0 conditions associated with rs606231422.
Pharmacogenetics
We do not have any data that links rs606231422 to any drugs.
Diagnostics
rs606231422 is commonly tested together with other variants on the same gene.
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 on gene CTLA4. 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.
Dr. Wallerstorfer
Conditions & Traits of rs606231422
Current research shows 0 conditions and 0 traits.
Diagnostics
rs606231422 is commonly tested together with other variants on the same gene.
Genotype Distribution
Knowing your genome can actually tell you a lot about your ancestors.
The prevalence of the different genotypes is based on the native inhabitants of a region. In the map below you see how common each genotype is in the native inhabitants of those regions. Since genetic material is passed down form generation to generation, your DNA shows traces of the geographical origins of your ancestors.
This data is based on “The 1000 Genomes Project” which established one of the most detailed overviews of human genetic variations across the globe. The regions are broadly categorized into five continental groups: Africa, America, Europe, South Asia and East Asia. All continental groups together display the global prevalence. Click through the regions, to learn more about the local prevalence of the possible genotypes.
At present, there is no distribution data available for SNP 606231422. 606231422.