Overview

rs634990 is a genetic variant.

This variant is located on chromosome 15. The variations at position 34713872 are the genetic letters A/A, C/C, G/G, T/T, A/C, C/G, G/T, A/T, A/G, 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 rs634990 there are 10 currently known genotypes : A/A, C/C, G/G, T/T, A/C, C/G, G/T, A/T, A/G or C/T

Short Overview

Variant Location

rs634990 is located on gene in chromsome 15. Use the genome browser to explore the location of rs634990 and its genetic neighbourhood.

Conditions & Traits

rs634990 affects the following conditions and traits:

There are currently 0 conditions and 0 traits associated with rs634990.

Pathogenicity

rs634990 affects the following conditions:

There are currently 0 conditions associated with rs634990.

Pharmacogenetics

We do not have any data that links rs634990 to any drugs.

Diagnostics

rs634990 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. 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

Conditions & Traits of rs634990

Current research shows 0 conditions and 0 traits.

Diagnostics

rs634990 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 634990. 634990.

The Genotype Distribution in the selected area is:
Legend:
Included regions
Excluded regions
no-data

Studies and Sources

All of the resources below examine variant rs634990

Regional replication of association with refractive error on 15q14 and 15q25 in the Age-Related Eye Disease Study cohort

Claire L. Simpson, Robert Wojciechowski, Stephanie S. Yee, Poorva Soni, Joan E. Bailey-Wilson, Dwight Stambolian

PMC: 3826323
Education influences the association between genetic variants and refractive error: a meta-analysis of five Singapore studies (1/15/14)

Qiao Fan, Robert Wojciechowski, M. Kamran Ikram, Ching-Yu Cheng, Peng Chen, Xin Zhou, Chen-Wei Pan, Chiea-Chuen Khor, E-Shyong Tai, Tin Aung, Tien-Yin Wong, Yik-Ying Teo, Seang-Mei Saw

PMC: 3869359
Association study of 15q14 and 15q25 with high myopia in the Han Chinese population

Yu Qiang, Wenjin Li, Qingzhong Wang, Kuanjun He, Zhiqiang Li, Jianhua Chen, Zhijian Song, Jia Qu, Xiangtian Zhou, Shengying Qin, Jiawei Shen, Zujia Wen, Jue Ji, Yongyong Shi

PMC: 4014749
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