Overview

rs10876864 is a genetic variant.

This variant is located on chromosome 12. The variations at position 56007301 are the genetic letters A/A, G/G, T/T, G/T, A/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 rs10876864 there are 6 currently known genotypes : A/A, G/G, T/T, G/T, A/T or A/G

Short Overview

Variant Location

rs10876864 is located on gene in chromsome 12. Use the genome browser to explore the location of rs10876864 and its genetic neighbourhood.

Conditions & Traits

rs10876864 affects the following conditions and traits:

There are currently 0 conditions and 0 traits associated with rs10876864.

Pathogenicity

rs10876864 affects the following conditions:

There are currently 0 conditions associated with rs10876864.

Pharmacogenetics

We do not have any data that links rs10876864 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.

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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 Dr. Wallerstorfer

Conditions & Traits of rs10876864

Current research shows 0 conditions and 0 traits.

Conditions

0

Studies and Sources

All of the resources below examine variant rs10876864

Genome-Wide Identification of Expression Quantitative Trait Loci (eQTLs) in Human Heart

Tamara T. Koopmann, Michiel E. Adriaens, Perry D. Moerland, Roos F. Marsman, Margriet L. Westerveld, Sean Lal, Taifang Zhang, Christine Q. Simmons, Istvan Baczko, Cristobal dos Remedios, Nanette H. Bishopric, Andras Varro, Alfred L. George, Elisabeth M. Lodder, Connie R. Bezzina

PMC: 4028258
Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci† (8/15/15)

Holger Kirsten, Hoor Al-Hasani, Lesca Holdt, Arnd Gross, Frank Beutner, Knut Krohn, Katrin Horn, Peter Ahnert, Ralph Burkhardt, Kristin Reiche, Jörg Hackermüller, Markus Löffler, Daniel Teupser, Joachim Thiery, Markus Scholz

PMC: 4512630
Genetic Susceptibility to Vitiligo: GWAS Approaches for Identifying Vitiligo Susceptibility Genes and Loci (2/1/16)

Changbing Shen, Jing Gao, Yujun Sheng, Jinfa Dou, Fusheng Zhou, Xiaodong Zheng, Randy Ko, Xianfa Tang, Caihong Zhu, Xianyong Yin, Liangdan Sun, Yong Cui, Xuejun Zhang

PMC: 4740779
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