rs10889677 is a genetic variant on gene IL23R.
This variant is located on chromosome 1. The variations at position 67259437 are the genetic letters A/A, C/C, T/T, A/C, A/T, C/T
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 rs10889677 there are 6 currently known genotypes : A/A, C/C, T/T, A/C, A/T or C/T
rs10889677 is located on gene IL23R in chromsome 1. Use the genome browser to explore the location of rs10889677 and its genetic neighbourhood.
rs10889677 affects the following conditions and traits:
There are currently 0 conditions and 0 traits associated with rs10889677.
rs10889677 affects the following conditions:
There are currently 0 conditions associated with rs10889677.
We do not have any data that links rs10889677 to any drugs.
rs10889677 is commonly tested together with other variants on the same gene.
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 IL23R. Explore more variants and their effects on the body by browsing left and right along the DNA strand.
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
Current research shows 0 conditions and 0 traits.
rs10889677 is commonly tested together with other variants on the same gene.
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 10889677. 10889677.
All of the resources below examine variant rs10889677
Jie-Jie Xu, Hai-Di Li, Xiao-Sa Du, Juan-Juan Li, Xiao-Ming Meng, Cheng Huang, Jun Li
Junfeng Zou, Chen Liu, Shu Jiang, Dawei Qian, Jinao Duan
Sefika Feyza Maden, Saliha Ece Acuner