Genetic variation
rs1057519893
Overview
rs1057519893 is a genetic variant on gene ERBB3.
This variant is located on chromosome 12. The variations at position 56085070 are the genetic letters A/A, G/G, T/T, G/T, 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 rs1057519893 there are 5 currently known genotypes : A/A, G/G, T/T, G/T or A/G
Short Overview
Variant Location
rs1057519893 is located on gene ERBB3 in chromsome 12. Use the genome browser to explore the location of rs1057519893 and its genetic neighbourhood.
Conditions & Traits
rs1057519893 affects the following conditions and traits:
There are currently 0 conditions and 0 traits associated with rs1057519893.
Pathogenicity
rs1057519893 affects the following conditions:
There are currently 0 conditions associated with rs1057519893.
Pharmacogenetics
We do not have any data that links rs1057519893 to any drugs.
Diagnostics
rs1057519893 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 ERBB3. 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 rs1057519893
Current research shows 0 conditions and 0 traits.
Diagnostics
rs1057519893 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 1057519893. 1057519893.