Genetic variation
rs267606611
Overview
rs267606611 is a genetic variant.
This variant is located on chromosome MT. The variations at position 9438 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 rs267606611 there are 3 currently known genotypes : A/A, G/G or A/G
Short Overview
Variant Location
rs267606611 is located on gene in chromsome MT. Use the genome browser to explore the location of rs267606611 and its genetic neighbourhood.
Conditions & Traits
rs267606611 affects the following conditions and traits:
There are currently 0 conditions and 0 traits associated with rs267606611.
Pathogenicity
rs267606611 affects the following conditions:
There are currently 0 conditions associated with rs267606611.
Pharmacogenetics
We do not have any data that links rs267606611 to any drugs.
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.
Dr. Wallerstorfer
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 267606611. 267606611.
Conditions & Traits of rs267606611
Current research shows 0 conditions and 0 traits.