Overview
rs10808546 is a genetic variant.
This variant is located on chromosome 8. The variations at position 125483576 are the genetic letters C/C, T/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 rs10808546 there are 3 currently known genotypes : C/C, T/T or C/T
Short Overview
Variant Location
rs10808546 is located on gene in chromsome 8. Use the genome browser to explore the location of rs10808546 and its genetic neighbourhood.
Conditions & Traits
rs10808546 affects the following conditions and traits:
There are currently 0 conditions and 0 traits associated with rs10808546.
Pathogenicity
rs10808546 affects the following conditions:
There are currently 0 conditions associated with rs10808546.
Pharmacogenetics
We do not have any data that links rs10808546 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.
Conditions & Traits of rs10808546
Current research shows 0 conditions and 0 traits.
Conditions
0Studies and Sources
All of the resources below examine variant rs10808546
Rachel L. Ballantyne, Xuan Zhang, Sara Nuñez, Chenyi Xue, Wei Zhao, Eric Reed, Danish Salaheen, Andrea S. Foulkes, Mingyao Li, Muredach P. Reilly