Overview

rs4236601 is a genetic variant.

This variant is located on chromosome 7. The variations at position 116522675 are the genetic letters A/A, G/G, 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 rs4236601 there are 3 currently known genotypes : A/A, G/G or A/G

Short Overview

Variant Location

rs4236601 is located on gene in chromsome 7. Use the genome browser to explore the location of rs4236601 and its genetic neighbourhood.

Conditions & Traits

rs4236601 affects the following conditions and traits:

There are currently 0 conditions and 0 traits associated with rs4236601.

Pathogenicity

rs4236601 affects the following conditions:

There are currently 0 conditions associated with rs4236601.

Pharmacogenetics

We do not have any data that links rs4236601 to any drugs.

Diagnostics

rs4236601 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 rs4236601

Current research shows 0 conditions and 0 traits.

Diagnostics

rs4236601 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 4236601. 4236601.

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 rs4236601

PMC: 6651941
Associations between TLR4 Polymorphisms and Open Angle Glaucoma: A Meta-Analysis

Zhongjing Lin, Shouyue Huang, Jun Sun, Bing Xie, Yisheng Zhong

PMC: 6681615
Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis (8/22/19)

Bao Jian Fan, Jessica Cooke Bailey, Rob P. Igo, Jae H. Kang, Tahani Boumenna, Murray H. Brilliant, Donald L. Budenz, John H. Fingert, Terry Gaasterland, Douglas Gaasterland, Michael A. Hauser, Peter Kraft, Richard K. Lee, Paul R. Lichter, Yutao Liu, Syoko E. Moroi, Jonathan S. Myers, Margaret A. Pericak-Vance, Anthony Realini, Douglas J. Rhee, Julia E. Richards, Robert Ritch, Joel S. Schuman, William K. Scott, Kuldev Singh, Arthur J. Sit, Douglas Vollrath, Robert N. Weinreb, Gadi Wollstein, Donald J. Zack, Jonathan L. Haines, Louis R. Pasquale, Janey L. Wiggs

PMC: 6707005
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